Canonical Allele Identifier: CA2584453458
Gene: HAMP HGNC NCBI

Linked Data

gnomAD v4: 19-35284879-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284879C>A , CM000681.2:g.35284879C>A GRCh38
NC_000019.9:g.35775782C>A , CM000681.1:g.35775782C>A GRCh37
NC_000019.8:g.40467622C>A NCBI36
NG_011563.1:g.7373C>A
NG_011563.2:g.7373C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.150+31C>A MANE Select ENSP00000222304.2:n.150+31C>A
ENST00000222304.3:c.150+31C>A ENSP00000222304.2:n.150+31C>A
ENST00000593580.1:n.2363C>A
ENST00000598398.5:c.150+31C>A ENSP00000471894.1:n.150+31C>A
NM_021175.2:c.150+31C>A NP_066998.1:n.150+31C>A
NM_021175.3:c.150+31C>A NP_066998.1:n.150+31C>A
NM_021175.4:c.150+31C>A MANE Select NP_066998.1:n.150+31C>A
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