Canonical Allele Identifier: CA361921542
Gene: HAND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477497C>G , CM000667.2:g.154477497C>G GRCh38
NC_000005.9:g.153857057C>G , CM000667.1:g.153857057C>G GRCh37
NC_000005.8:g.153837250C>G NCBI36
NG_052889.1:g.5768G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.512G>C MANE Select ENSP00000231121.2:p.Gly171Ala
ENST00000231121.2:c.512G>C ENSP00000231121.2:p.Gly171Ala
NM_004821.2:c.512G>C NP_004812.1:p.Gly171Ala
XM_005268531.1:c.512G>C XP_005268588.1:p.Gly171Ala
NM_004821.3:c.512G>C MANE Select NP_004812.1:p.Gly171Ala