Canonical Allele Identifier: CA2676143103
Gene: HAND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477361C>A , CM000667.2:g.154477361C>A GRCh38
NC_000005.9:g.153856921C>A , CM000667.1:g.153856921C>A GRCh37
NC_000005.8:g.153837114C>A NCBI36
NG_052889.1:g.5904G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.543+105G>T MANE Select ENSP00000231121.2:n.543+105G>T
ENST00000231121.2:c.543+105G>T ENSP00000231121.2:n.543+105G>T
NM_004821.2:c.543+105G>T NP_004812.1:n.543+105G>T
XM_005268531.1:c.543+105G>T XP_005268588.1:n.543+105G>T
NM_004821.3:c.543+105G>T MANE Select NP_004812.1:n.543+105G>T