Canonical Allele Identifier: CA454513111
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs766125491
MyVariant Identifiers: chr7:g.27237892C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198273C>T , CM000669.2:g.27198273C>T GRCh38
NC_000007.13:g.27237892C>T , CM000669.1:g.27237892C>T GRCh37
NC_000007.12:g.27204417C>T NCBI36
NG_008181.1:g.6834G>A
NG_008181.2:g.6834G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.1092G>A MANE Select ENSP00000497112.1:p.Arg364=
ENST00000222753.5:c.1092G>A ENSP00000222753.4:p.Arg364=
NM_000522.4:c.1092G>A NP_000513.2:p.Arg364=
XM_011515344.1:c.1092G>A XP_011513646.1:p.Arg364=
NM_000522.5:c.1092G>A MANE Select NP_000513.2:p.Arg364=
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