Canonical Allele Identifier: CA2576753472
Gene: HAMP HGNC NCBI

Linked Data

gnomAD v4: 19-35285116-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35285116A>G , CM000681.2:g.35285116A>G GRCh38
NC_000019.9:g.35776019A>G , CM000681.1:g.35776019A>G GRCh37
NC_000019.8:g.40467859A>G NCBI36
NG_011563.1:g.7610A>G
NG_011563.2:g.7610A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.*74A>G MANE Select ENSP00000222304.2:n.*74A>G
ENST00000593580.1:n.2600A>G
ENST00000598398.5:c.*74A>G ENSP00000471894.1:n.*74A>G
NM_021175.2:c.*74A>G NP_066998.1:n.*74A>G
NM_021175.3:c.*74A>G NP_066998.1:n.*74A>G
NM_021175.4:c.*74A>G MANE Select NP_066998.1:n.*74A>G
Search 100 bp 5'
Search 100 bp 3'