Canonical Allele Identifier: CA447421571
Gene: HAND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.153857086G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477526G>T , CM000667.2:g.154477526G>T GRCh38
NC_000005.9:g.153857086G>T , CM000667.1:g.153857086G>T GRCh37
NC_000005.8:g.153837279G>T NCBI36
NG_052889.1:g.5739C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.483C>A MANE Select ENSP00000231121.2:p.Ala161=
ENST00000231121.2:c.483C>A ENSP00000231121.2:p.Ala161=
NM_004821.2:c.483C>A NP_004812.1:p.Ala161=
XM_005268531.1:c.483C>A XP_005268588.1:p.Ala161=
NM_004821.3:c.483C>A MANE Select NP_004812.1:p.Ala161=
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