Canonical Allele Identifier: CA405300839
Gene: HAMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284836G>T , CM000681.2:g.35284836G>T GRCh38
NC_000019.9:g.35775739G>T , CM000681.1:g.35775739G>T GRCh37
NC_000019.8:g.40467579G>T NCBI36
NG_011563.1:g.7330G>T
NG_011563.2:g.7330G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.138G>T MANE Select ENSP00000222304.2:p.Arg46Ser
ENST00000222304.3:c.138G>T ENSP00000222304.2:p.Arg46Ser
ENST00000593580.1:n.2320G>T
ENST00000598398.5:c.138G>T ENSP00000471894.1:p.Arg46Ser
NM_021175.2:c.138G>T NP_066998.1:p.Arg46Ser
NM_021175.3:c.138G>T NP_066998.1:p.Arg46Ser
NM_021175.4:c.138G>T MANE Select NP_066998.1:p.Arg46Ser