Canonical Allele Identifier: CA13758508
Gene: HIGD1C HGNC NCBI
SLC11A2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12304921

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.50963759A>G , CM000674.2:g.50963759A>G GRCh38
NC_000012.11:g.51357542A>G , CM000674.1:g.51357542A>G GRCh37
NC_000012.10:g.49643809A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001109619.1:n.229+2657A>G (HIGD1C) VV NP_001103089.1:p.=
XM_011538648.1:c.544+2657A>G (HIGD1C) XP_011536950.1:p.=
XM_011538649.1:c.229+2657A>G (HIGD1C) XP_011536951.1:p.=
NM_001109619.2:c.229+2657A>G (HIGD1C) VV NP_001103089.1:p.=
XM_011538649.2:c.229+2657A>G (HIGD1C) XP_011536951.1:p.=
XM_017019783.2:c.373+2657A>G (HIGD1C) XP_016875272.1:p.=
XM_017019784.2:c.373+2657A>G (HIGD1C) XP_016875273.1:p.=
XM_017019785.1:c.253+2657A>G (HIGD1C) XP_016875274.1:p.=
XR_001748720.1:n.1992-9951T>C (SLC11A2)
ENST00000398455.3:c.229+2657A>G ENSP00000381473.3:p.=