Canonical Allele Identifier: CA1592792815
Gene: HAND1 HGNC NCBI

Linked Data

dbSNP Id: rs1561711253

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477394A>G , CM000667.2:g.154477394A>G GRCh38
NC_000005.9:g.153856954A>G , CM000667.1:g.153856954A>G GRCh37
NC_000005.8:g.153837147A>G NCBI36
NG_052889.1:g.5871T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.543+72T>C MANE Select ENSP00000231121.2:n.543+72T>C
ENST00000231121.2:c.543+72T>C ENSP00000231121.2:n.543+72T>C
NM_004821.2:c.543+72T>C NP_004812.1:n.543+72T>C
XM_005268531.1:c.543+72T>C XP_005268588.1:n.543+72T>C
NM_004821.3:c.543+72T>C MANE Select NP_004812.1:n.543+72T>C