Canonical Allele Identifier: CA349988392

Gene: SLC40A1

Linked Data

• dbSNP Id: rs104893664
• MyVariant Identifiers: chr2:g.190428912C>A (hg19) ; chr2:g.189564186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189564186C>A , CM000664.2:g.189564186C>A	GRCh38
NC_000002.11:g.190428912C>A , CM000664.1:g.190428912C>A	GRCh37
NC_000002.10:g.190137157C>A	NCBI36
NG_009027.1:g.21626G>T , LRG_837:g.21626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.800G>T MANE Select	ENSP00000261024.3:p.Gly267Val
ENST00000261024.6:c.800G>T	ENSP00000261024.2:p.Gly267Val
NM_014585.5:c.800G>T , LRG_837t1:c.800G>T	NP_055400.1:p.Gly267Val
XM_005246505.1:c.680G>T	XP_005246562.1:p.Gly227Val
XM_005246505.2:c.680G>T	XP_005246562.1:p.Gly227Val
XM_017003938.2:c.680G>T	XP_016859427.1:p.Gly227Val
NM_014585.6:c.800G>T MANE Select	NP_055400.1:p.Gly267Val