Canonical Allele Identifier: CA361921483
Gene: HAND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.153857043T>A (hg19) chr5:g.154477483T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477483T>A , CM000667.2:g.154477483T>A GRCh38
NC_000005.9:g.153857043T>A , CM000667.1:g.153857043T>A GRCh37
NC_000005.8:g.153837236T>A NCBI36
NG_052889.1:g.5782A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000231121.3:c.526A>T MANE Select ENSP00000231121.2:p.Lys176Ter
ENST00000231121.2:c.526A>T ENSP00000231121.2:p.Lys176Ter
NM_004821.2:c.526A>T NP_004812.1:p.Lys176Ter
XM_005268531.1:c.526A>T XP_005268588.1:p.Lys176Ter
NM_004821.3:c.526A>T MANE Select NP_004812.1:p.Lys176Ter
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