Canonical Allele Identifier: CA421938665

Linked Data

MyVariant Identifiers: chr1:g.171605245T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636105T>C , CM000663.2:g.171636105T>C GRCh38
NC_000001.10:g.171605245T>C , CM000663.1:g.171605245T>C GRCh37
NC_000001.9:g.169871868T>C NCBI36
NG_008859.1:g.21529A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1335A>G (MYOC) MANE Select ENSP00000037502.5:p.Ala445=
ENST00000637303.1:c.235-2525T>C (MYOCOS) ENSP00000490048.1:n.235-2525T>C
ENST00000638471.1:c.*673A>G (MYOC) ENSP00000491206.1:n.*673A>G
ENST00000037502.10:c.1335A>G (MYOC) ENSP00000037502.5:p.Ala445=
ENST00000614688.1:c.*299A>G (MYOC) ENSP00000478680.1:n.*299A>G
NM_000261.1:c.1335A>G (MYOC) NP_000252.1:p.Ala445=
NM_000261.2:c.1335A>G (MYOC) MANE Select NP_000252.1:p.Ala445=