Canonical Allele Identifier: CA405300748
Gene: HAMP HGNC NCBI

Linked Data

dbSNP Id: rs145850917
MyVariant Identifiers: chr19:g.35775729C>A (hg19) chr19:g.35284826C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284826C>A , CM000681.2:g.35284826C>A GRCh38
NC_000019.9:g.35775729C>A , CM000681.1:g.35775729C>A GRCh37
NC_000019.8:g.40467569C>A NCBI36
NG_011563.1:g.7320C>A
NG_011563.2:g.7320C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.128C>A MANE Select ENSP00000222304.2:p.Ala43Asp
ENST00000222304.3:c.128C>A ENSP00000222304.2:p.Ala43Asp
ENST00000593580.1:n.2310C>A
ENST00000598398.5:c.128C>A ENSP00000471894.1:p.Ala43Asp
NM_021175.2:c.128C>A NP_066998.1:p.Ala43Asp
NM_021175.3:c.128C>A NP_066998.1:p.Ala43Asp
NM_021175.4:c.128C>A MANE Select NP_066998.1:p.Ala43Asp
Search 100 bp 5'
Search 100 bp 3'