Canonical Allele Identifier: CA454513123
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115471192
MyVariant Identifiers: chr7:g.27237898A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198279A>T , CM000669.2:g.27198279A>T GRCh38
NC_000007.13:g.27237898A>T , CM000669.1:g.27237898A>T GRCh37
NC_000007.12:g.27204423A>T NCBI36
NG_008181.1:g.6828T>A
NG_008181.2:g.6828T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.1086T>A MANE Select ENSP00000497112.1:p.Ser362=
ENST00000222753.5:c.1086T>A ENSP00000222753.4:p.Ser362=
NM_000522.4:c.1086T>A NP_000513.2:p.Ser362=
XM_011515344.1:c.1086T>A XP_011513646.1:p.Ser362=
NM_000522.5:c.1086T>A MANE Select NP_000513.2:p.Ser362=
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