Canonical Allele Identifier: CA367069673
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115471154

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198265G>T , CM000669.2:g.27198265G>T GRCh38
NC_000007.13:g.27237884G>T , CM000669.1:g.27237884G>T GRCh37
NC_000007.12:g.27204409G>T NCBI36
NG_008181.1:g.6842C>A
NG_008181.2:g.6842C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.1100C>A MANE Select ENSP00000497112.1:p.Thr367Lys
ENST00000222753.5:c.1100C>A ENSP00000222753.4:p.Thr367Lys
NM_000522.4:c.1100C>A NP_000513.2:p.Thr367Lys
XM_011515344.1:c.1100C>A XP_011513646.1:p.Thr367Lys
NM_000522.5:c.1100C>A MANE Select NP_000513.2:p.Thr367Lys