Canonical Allele Identifier: CA361921733
Gene: HAND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477524A>T , CM000667.2:g.154477524A>T GRCh38
NC_000005.9:g.153857084A>T , CM000667.1:g.153857084A>T GRCh37
NC_000005.8:g.153837277A>T NCBI36
NG_052889.1:g.5741T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.485T>A MANE Select ENSP00000231121.2:p.Phe162Tyr
ENST00000231121.2:c.485T>A ENSP00000231121.2:p.Phe162Tyr
NM_004821.2:c.485T>A NP_004812.1:p.Phe162Tyr
XM_005268531.1:c.485T>A XP_005268588.1:p.Phe162Tyr
NM_004821.3:c.485T>A MANE Select NP_004812.1:p.Phe162Tyr