Canonical Allele Identifier: CA2768994034
Gene: HAND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477375G>A , CM000667.2:g.154477375G>A GRCh38
NC_000005.9:g.153856935G>A , CM000667.1:g.153856935G>A GRCh37
NC_000005.8:g.153837128G>A NCBI36
NG_052889.1:g.5890C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.543+91C>T MANE Select ENSP00000231121.2:n.543+91C>T
ENST00000231121.2:c.543+91C>T ENSP00000231121.2:n.543+91C>T
NM_004821.2:c.543+91C>T NP_004812.1:n.543+91C>T
XM_005268531.1:c.543+91C>T XP_005268588.1:n.543+91C>T
NM_004821.3:c.543+91C>T MANE Select NP_004812.1:n.543+91C>T