Canonical Allele Identifier: CA1592792957
Gene: HAND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477491C= , CM000667.2:g.154477491C= GRCh38
NC_000005.9:g.153857051C= , CM000667.1:g.153857051C= GRCh37
NC_000005.8:g.153837244C= NCBI36
NG_052889.1:g.5774G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.518G= MANE Select ENSP00000231121.2:p.Arg173=
ENST00000231121.2:c.518G= ENSP00000231121.2:p.Arg173=
NM_004821.2:c.518G= NP_004812.1:p.Arg173=
XM_005268531.1:c.518G= XP_005268588.1:p.Arg173=
NM_004821.3:c.518G= MANE Select NP_004812.1:p.Arg173=