Canonical Allele Identifier: CA2123466282

Linked Data

dbSNP Id: rs1892209706

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416324T>A , CM000676.2:g.23416324T>A GRCh38
NC_000014.8:g.23885533T>A , CM000676.1:g.23885533T>A GRCh37
NC_000014.7:g.22955373T>A NCBI36
NG_007884.1:g.24338A>T , LRG_384:g.24338A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4645-12A>T (MYH7) MANE Select ENSP00000347507.3:n.4645-12A>T
ENST00000355349.3:c.4645-12A>T (MYH7) ENSP00000347507.3:n.4645-12A>T
NM_000257.3:c.4645-12A>T (MYH7) NP_000248.2:n.4645-12A>T
NR_126491.1:n.558+27T>A (MHRT)
XM_017021340.1:c.4645-12A>T (MYH7) XP_016876829.1:n.4645-12A>T
NM_000257.4:c.4645-12A>T (MYH7) MANE Select NP_000248.2:n.4645-12A>T