Canonical Allele Identifier: CA2333584678
Gene: HAMP HGNC NCBI

Linked Data

dbSNP Id: rs1204396318
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35281997C>A , CM000681.2:g.35281997C>A GRCh38
NC_000019.9:g.35772900C>A , CM000681.1:g.35772900C>A GRCh37
NC_000019.8:g.40464740C>A NCBI36
NG_011563.1:g.4491C>A
NG_011563.2:g.4491C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000598398.5:c.-84-497C>A ENSP00000471894.1:n.-84-497C>A
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