Canonical Allele Identifier: CA1592792950
Gene: HAND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477488T= , CM000667.2:g.154477488T= GRCh38
NC_000005.9:g.153857048T= , CM000667.1:g.153857048T= GRCh37
NC_000005.8:g.153837241T= NCBI36
NG_052889.1:g.5777A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.521A= MANE Select ENSP00000231121.2:p.Glu174=
ENST00000231121.2:c.521A= ENSP00000231121.2:p.Glu174=
NM_004821.2:c.521A= NP_004812.1:p.Glu174=
XM_005268531.1:c.521A= XP_005268588.1:p.Glu174=
NM_004821.3:c.521A= MANE Select NP_004812.1:p.Glu174=