Canonical Allele Identifier: CA130059551
Gene: HAND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1282978
ClinVar RCV Id: RCV001689237
dbSNP Id: rs112556829

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477396T>C , CM000667.2:g.154477396T>C GRCh38
NC_000005.9:g.153856956T>C , CM000667.1:g.153856956T>C GRCh37
NC_000005.8:g.153837149T>C NCBI36
NG_052889.1:g.5869A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.543+70A>G MANE Select ENSP00000231121.2:n.543+70A>G
ENST00000231121.2:c.543+70A>G ENSP00000231121.2:n.543+70A>G
NM_004821.2:c.543+70A>G NP_004812.1:n.543+70A>G
XM_005268531.1:c.543+70A>G XP_005268588.1:n.543+70A>G
NM_004821.3:c.543+70A>G MANE Select NP_004812.1:n.543+70A>G