Canonical Allele Identifier: CA1592792881
Gene: HAND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477441G= , CM000667.2:g.154477441G= GRCh38
NC_000005.9:g.153857001G= , CM000667.1:g.153857001G= GRCh37
NC_000005.8:g.153837194G= NCBI36
NG_052889.1:g.5824C=

Transcript Alleles

HGVS Amino-acid change
ENST00000231121.3:c.543+25C= MANE Select ENSP00000231121.2:n.543+25C=
ENST00000231121.2:c.543+25C= ENSP00000231121.2:n.543+25C=
NM_004821.2:c.543+25C= NP_004812.1:n.543+25C=
XM_005268531.1:c.543+25C= XP_005268588.1:n.543+25C=
NM_004821.3:c.543+25C= MANE Select NP_004812.1:n.543+25C=