Canonical Allele Identifier: CA2714008364
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115471001

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198196C>A , CM000669.2:g.27198196C>A GRCh38
NC_000007.13:g.27237815C>A , CM000669.1:g.27237815C>A GRCh37
NC_000007.12:g.27204340C>A NCBI36
NG_008181.1:g.6911G>T
NG_008181.2:g.6911G>T

Transcript Alleles

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