Canonical Allele Identifier: CA307740313
Gene: HAMP HGNC NCBI

Linked Data

dbSNP Id: rs111878333
MyVariant Identifiers: chr19:g.35775838C>A (hg19) chr19:g.35284935C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284935C>A , CM000681.2:g.35284935C>A GRCh38
NC_000019.9:g.35775838C>A , CM000681.1:g.35775838C>A GRCh37
NC_000019.8:g.40467678C>A NCBI36
NG_011563.1:g.7429C>A
NG_011563.2:g.7429C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000222304.5:c.151-3C>A MANE Select ENSP00000222304.2:n.151-3C>A
ENST00000222304.3:c.151-3C>A ENSP00000222304.2:n.151-3C>A
ENST00000593580.1:n.2419C>A
ENST00000598398.5:c.151-3C>A ENSP00000471894.1:n.151-3C>A
NM_021175.2:c.151-3C>A NP_066998.1:n.151-3C>A
NM_021175.3:c.151-3C>A NP_066998.1:n.151-3C>A
NM_021175.4:c.151-3C>A MANE Select NP_066998.1:n.151-3C>A
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