Canonical Allele Identifier: CA1592792889
Gene: HAND1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477447T= , CM000667.2:g.154477447T= GRCh38
NC_000005.9:g.153857007T= , CM000667.1:g.153857007T= GRCh37
NC_000005.8:g.153837200T= NCBI36
NG_052889.1:g.5818A=

Transcript Alleles

HGVS Amino-acid change
ENST00000231121.3:c.543+19A= MANE Select ENSP00000231121.2:n.543+19A=
ENST00000231121.2:c.543+19A= ENSP00000231121.2:n.543+19A=
NM_004821.2:c.543+19A= NP_004812.1:n.543+19A=
XM_005268531.1:c.543+19A= XP_005268588.1:n.543+19A=
NM_004821.3:c.543+19A= MANE Select NP_004812.1:n.543+19A=
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