Canonical Allele Identifier: CA881771487

Gene: HAMP

Linked Data

• dbSNP Id: rs1280512772
• gnomAD v4: 19-35284874-T-C
• MyVariant Identifiers: chr19:g.35775777T>C (hg19) ; chr19:g.35284874T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284874T>C , CM000681.2:g.35284874T>C	GRCh38
NC_000019.9:g.35775777T>C , CM000681.1:g.35775777T>C	GRCh37
NC_000019.8:g.40467617T>C	NCBI36
NG_011563.1:g.7368T>C
NG_011563.2:g.7368T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.150+26T>C MANE Select	ENSP00000222304.2:n.150+26T>C
ENST00000222304.3:c.150+26T>C	ENSP00000222304.2:n.150+26T>C
ENST00000593580.1:n.2358T>C
ENST00000598398.5:c.150+26T>C	ENSP00000471894.1:n.150+26T>C
NM_021175.2:c.150+26T>C	NP_066998.1:n.150+26T>C
NM_021175.3:c.150+26T>C	NP_066998.1:n.150+26T>C
NM_021175.4:c.150+26T>C MANE Select	NP_066998.1:n.150+26T>C