Canonical Allele Identifier: CA405300617

Gene: HAMP

Linked Data

• MyVariant Identifiers: chr19:g.35775716C>G (hg19) ; chr19:g.35284813C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284813C>G , CM000681.2:g.35284813C>G	GRCh38
NC_000019.9:g.35775716C>G , CM000681.1:g.35775716C>G	GRCh37
NC_000019.8:g.40467556C>G	NCBI36
NG_011563.1:g.7307C>G
NG_011563.2:g.7307C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.115C>G MANE Select	ENSP00000222304.2:p.Pro39Ala
ENST00000222304.3:c.115C>G	ENSP00000222304.2:p.Pro39Ala
ENST00000593580.1:n.2297C>G
ENST00000598398.5:c.115C>G	ENSP00000471894.1:p.Pro39Ala
NM_021175.2:c.115C>G	NP_066998.1:p.Pro39Ala
NM_021175.3:c.115C>G	NP_066998.1:p.Pro39Ala
NM_021175.4:c.115C>G MANE Select	NP_066998.1:p.Pro39Ala