Canonical Allele Identifier: CA764878559

Gene: SLC11A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218381984C>A , CM000664.2:g.218381984C>A	GRCh38
NC_000002.11:g.219246707C>A , CM000664.1:g.219246707C>A	GRCh37
NC_000002.10:g.218954951C>A	NCBI36
NG_012128.1:g.4956C>A

Transcript Alleles

HGVS	Amino-acid Change
XM_005246793.2:c.-443C>A	XP_005246850.1:n.-443C>A
XM_005246794.2:c.-813C>A	XP_005246851.1:n.-813C>A
XM_006712709.2:c.-670C>A	XP_006712772.1:n.-670C>A
XM_006712710.2:c.-547C>A	XP_006712773.1:n.-547C>A
XM_006712711.2:c.-566C>A	XP_006712774.1:n.-566C>A
XM_011511684.1:c.-821C>A	XP_011509986.1:n.-821C>A
XM_011511685.1:c.-678C>A	XP_011509987.1:n.-678C>A
XR_427108.2:n.219C>A
XM_005246793.4:c.-443C>A	XP_005246850.1:n.-443C>A
XM_005246794.4:c.-813C>A	XP_005246851.1:n.-813C>A
XM_006712709.4:c.-670C>A	XP_006712772.1:n.-670C>A
XM_006712710.4:c.-547C>A	XP_006712773.1:n.-547C>A
XM_006712711.4:c.-566C>A	XP_006712774.1:n.-566C>A
XM_011511684.3:c.-821C>A	XP_011509986.1:n.-821C>A
XM_011511685.3:c.-678C>A	XP_011509987.1:n.-678C>A
XM_017004765.2:c.-385C>A	XP_016860254.1:n.-385C>A
XM_017004766.2:c.-554C>A	XP_016860255.1:n.-554C>A
XR_427108.4:n.219C>A