Canonical Allele Identifier: CA1592793049
Gene: HAND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477557G= , CM000667.2:g.154477557G= GRCh38
NC_000005.9:g.153857117G= , CM000667.1:g.153857117G= GRCh37
NC_000005.8:g.153837310G= NCBI36
NG_052889.1:g.5708C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.452C= MANE Select ENSP00000231121.2:p.Ala151=
ENST00000231121.2:c.452C= ENSP00000231121.2:p.Ala151=
NM_004821.2:c.452C= NP_004812.1:p.Ala151=
XM_005268531.1:c.452C= XP_005268588.1:p.Ala151=
NM_004821.3:c.452C= MANE Select NP_004812.1:p.Ala151=