Canonical Allele Identifier: CA2682147469
Gene: HOXA13 HGNC NCBI

Linked Data

gnomAD v4: 7-27198074-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198074C>A , CM000669.2:g.27198074C>A GRCh38
NC_000007.13:g.27237693C>A , CM000669.1:g.27237693C>A GRCh37
NC_000007.12:g.27204218C>A NCBI36
NG_008181.1:g.7033G>T
NG_008181.2:g.7033G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.*124G>T MANE Select ENSP00000497112.1:n.*124G>T
ENST00000222753.5:c.*124G>T ENSP00000222753.4:n.*124G>T
NM_000522.4:c.*124G>T NP_000513.2:n.*124G>T
XM_011515344.1:c.*124G>T XP_011513646.1:n.*124G>T
NM_000522.5:c.*124G>T MANE Select NP_000513.2:n.*124G>T
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