Canonical Allele Identifier: CA2584453446
Gene: HAMP HGNC NCBI

Linked Data

gnomAD v4: 19-35284857-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284857A>G , CM000681.2:g.35284857A>G GRCh38
NC_000019.9:g.35775760A>G , CM000681.1:g.35775760A>G GRCh37
NC_000019.8:g.40467600A>G NCBI36
NG_011563.1:g.7351A>G
NG_011563.2:g.7351A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.150+9A>G MANE Select ENSP00000222304.2:n.150+9A>G
ENST00000222304.3:c.150+9A>G ENSP00000222304.2:n.150+9A>G
ENST00000593580.1:n.2341A>G
ENST00000598398.5:c.150+9A>G ENSP00000471894.1:n.150+9A>G
NM_021175.2:c.150+9A>G NP_066998.1:n.150+9A>G
NM_021175.3:c.150+9A>G NP_066998.1:n.150+9A>G
NM_021175.4:c.150+9A>G MANE Select NP_066998.1:n.150+9A>G
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