Canonical Allele Identifier: CA349353156
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs2105379123

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093524A>T , CM000664.2:g.176093524A>T GRCh38
NC_000002.11:g.176958252A>T , CM000664.1:g.176958252A>T GRCh37
NC_000002.10:g.176666498A>T NCBI36
NG_008137.1:g.5721A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.634A>T MANE Select ENSP00000376322.3:p.Thr212Ser
ENST00000392539.3:c.634A>T ENSP00000376322.3:p.Thr212Ser
NM_000523.3:c.634A>T NP_000514.2:p.Thr212Ser
XM_011511068.1:c.725-956A>T XP_011509370.1:n.725-956A>T
XM_011511068.2:c.725-956A>T XP_011509370.1:n.725-956A>T
NM_000523.4:c.634A>T MANE Select NP_000514.2:p.Thr212Ser