Canonical Allele Identifier: CA2581380875
Gene: HAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35281996A>C , CM000681.2:g.35281996A>C GRCh38
NC_000019.9:g.35772899A>C , CM000681.1:g.35772899A>C GRCh37
NC_000019.8:g.40464739A>C NCBI36
NG_011563.1:g.4490A>C
NG_011563.2:g.4490A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000598398.5:c.-84-498A>C ENSP00000471894.1:n.-84-498A>C