Canonical Allele Identifier: CA507041354

Gene: HAMP

Linked Data

• MyVariant Identifiers: chr19:g.35775853A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284950A>C , CM000681.2:g.35284950A>C	GRCh38
NC_000019.9:g.35775853A>C , CM000681.1:g.35775853A>C	GRCh37
NC_000019.8:g.40467693A>C	NCBI36
NG_011563.1:g.7444A>C
NG_011563.2:g.7444A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.163A>C MANE Select	ENSP00000222304.2:p.Arg55=
ENST00000222304.3:c.163A>C	ENSP00000222304.2:p.Arg55=
ENST00000593580.1:n.2434A>C
ENST00000598398.5:c.163A>C	ENSP00000471894.1:p.Arg55=
NM_021175.2:c.163A>C	NP_066998.1:p.Arg55=
NM_021175.3:c.163A>C	NP_066998.1:p.Arg55=
NM_021175.4:c.163A>C MANE Select	NP_066998.1:p.Arg55=