Canonical Allele Identifier: CA447421469
Gene: HAND1 HGNC NCBI

Linked Data

dbSNP Id: rs1582056866
MyVariant Identifiers: chr5:g.153857050A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477490A>C , CM000667.2:g.154477490A>C GRCh38
NC_000005.9:g.153857050A>C , CM000667.1:g.153857050A>C GRCh37
NC_000005.8:g.153837243A>C NCBI36
NG_052889.1:g.5775T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000231121.3:c.519T>G MANE Select ENSP00000231121.2:p.Arg173=
ENST00000231121.2:c.519T>G ENSP00000231121.2:p.Arg173=
NM_004821.2:c.519T>G NP_004812.1:p.Arg173=
XM_005268531.1:c.519T>G XP_005268588.1:p.Arg173=
NM_004821.3:c.519T>G MANE Select NP_004812.1:p.Arg173=
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