Canonical Allele Identifier: CA361921587
Gene: HAND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477500T>A , CM000667.2:g.154477500T>A GRCh38
NC_000005.9:g.153857060T>A , CM000667.1:g.153857060T>A GRCh37
NC_000005.8:g.153837253T>A NCBI36
NG_052889.1:g.5765A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.509A>T MANE Select ENSP00000231121.2:p.Asp170Val
ENST00000231121.2:c.509A>T ENSP00000231121.2:p.Asp170Val
NM_004821.2:c.509A>T NP_004812.1:p.Asp170Val
XM_005268531.1:c.509A>T XP_005268588.1:p.Asp170Val
NM_004821.3:c.509A>T MANE Select NP_004812.1:p.Asp170Val