Canonical Allele Identifier: CA4198545
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs766983635
gnomAD v3: 7-27198264-T-C
gnomAD v4: 7-27198264-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198264T>C , CM000669.2:g.27198264T>C GRCh38
NC_000007.13:g.27237883T>C , CM000669.1:g.27237883T>C GRCh37
NC_000007.12:g.27204408T>C NCBI36
NG_008181.1:g.6843A>G
NG_008181.2:g.6843A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.1101A>G MANE Select ENSP00000497112.1:p.Thr367=
ENST00000222753.5:c.1101A>G ENSP00000222753.4:p.Thr367=
NM_000522.4:c.1101A>G NP_000513.2:p.Thr367=
XM_011515344.1:c.1101A>G XP_011513646.1:p.Thr367=
NM_000522.5:c.1101A>G MANE Select NP_000513.2:p.Thr367=