Canonical Allele Identifier: CA2714008316
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115470986
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198188T>A , CM000669.2:g.27198188T>A GRCh38
NC_000007.13:g.27237807T>A , CM000669.1:g.27237807T>A GRCh37
NC_000007.12:g.27204332T>A NCBI36
NG_008181.1:g.6919A>T
NG_008181.2:g.6919A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*10A>T MANE Select ENSP00000497112.1:n.*10A>T
ENST00000222753.5:c.*10A>T ENSP00000222753.4:n.*10A>T
NM_000522.4:c.*10A>T NP_000513.2:n.*10A>T
XM_011515344.1:c.*10A>T XP_011513646.1:n.*10A>T
NM_000522.5:c.*10A>T MANE Select NP_000513.2:n.*10A>T
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