Canonical Allele Identifier: CA2713835376
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs757359297
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198173G>T , CM000669.2:g.27198173G>T GRCh38
NC_000007.13:g.27237792G>T , CM000669.1:g.27237792G>T GRCh37
NC_000007.12:g.27204317G>T NCBI36
NG_008181.1:g.6934C>A
NG_008181.2:g.6934C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*25C>A MANE Select ENSP00000497112.1:n.*25C>A
ENST00000222753.5:c.*25C>A ENSP00000222753.4:n.*25C>A
NM_000522.4:c.*25C>A NP_000513.2:n.*25C>A
XM_011515344.1:c.*25C>A XP_011513646.1:n.*25C>A
NM_000522.5:c.*25C>A MANE Select NP_000513.2:n.*25C>A
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