Canonical Allele Identifier: CA507041096
Gene: HAMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.35775721G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284818G>A , CM000681.2:g.35284818G>A GRCh38
NC_000019.9:g.35775721G>A , CM000681.1:g.35775721G>A GRCh37
NC_000019.8:g.40467561G>A NCBI36
NG_011563.1:g.7312G>A
NG_011563.2:g.7312G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.120G>A MANE Select ENSP00000222304.2:p.Gln40=
ENST00000222304.3:c.120G>A ENSP00000222304.2:p.Gln40=
ENST00000593580.1:n.2302G>A
ENST00000598398.5:c.120G>A ENSP00000471894.1:p.Gln40=
NM_021175.2:c.120G>A NP_066998.1:p.Gln40=
NM_021175.3:c.120G>A NP_066998.1:p.Gln40=
NM_021175.4:c.120G>A MANE Select NP_066998.1:p.Gln40=