Canonical Allele Identifier: CA9375810

Gene: HAMP

Linked Data

• dbSNP Id: rs759921570
• ExAC: 19:35775807 C / A
• gnomAD v2: 19-35775807-C-A
• gnomAD v4: 19-35284904-C-A
• MyVariant Identifiers: chr19:g.35775807C>A (hg19) ; chr19:g.35284904C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284904C>A , CM000681.2:g.35284904C>A	GRCh38
NC_000019.9:g.35775807C>A , CM000681.1:g.35775807C>A	GRCh37
NC_000019.8:g.40467647C>A	NCBI36
NG_011563.1:g.7398C>A
NG_011563.2:g.7398C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222304.5:c.151-34C>A MANE Select	ENSP00000222304.2:n.151-34C>A
ENST00000222304.3:c.151-34C>A	ENSP00000222304.2:n.151-34C>A
ENST00000593580.1:n.2388C>A
ENST00000598398.5:c.151-34C>A	ENSP00000471894.1:n.151-34C>A
NM_021175.2:c.151-34C>A	NP_066998.1:n.151-34C>A
NM_021175.3:c.151-34C>A	NP_066998.1:n.151-34C>A
NM_021175.4:c.151-34C>A MANE Select	NP_066998.1:n.151-34C>A