Canonical Allele Identifier: CA1592792852
Gene: HAND1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477427C= , CM000667.2:g.154477427C= GRCh38
NC_000005.9:g.153856987C= , CM000667.1:g.153856987C= GRCh37
NC_000005.8:g.153837180C= NCBI36
NG_052889.1:g.5838G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.543+39G= MANE Select ENSP00000231121.2:n.543+39G=
ENST00000231121.2:c.543+39G= ENSP00000231121.2:n.543+39G=
NM_004821.2:c.543+39G= NP_004812.1:n.543+39G=
XM_005268531.1:c.543+39G= XP_005268588.1:n.543+39G=
NM_004821.3:c.543+39G= MANE Select NP_004812.1:n.543+39G=
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