Canonical Allele Identifier: CA349989750
Gene: SLC40A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.190439965C>G (hg19) chr2:g.189575239C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575239C>G , CM000664.2:g.189575239C>G GRCh38
NC_000002.11:g.190439965C>G , CM000664.1:g.190439965C>G GRCh37
NC_000002.10:g.190148210C>G NCBI36
NG_009027.1:g.10573G>C , LRG_837:g.10573G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.193G>C MANE Select ENSP00000261024.3:p.Gly65Arg
ENST00000261024.6:c.193G>C ENSP00000261024.2:p.Gly65Arg
ENST00000418714.1:n.634G>C
ENST00000427241.5:c.193G>C ENSP00000390005.1:p.Gly65Arg
ENST00000479598.5:n.474G>C
NM_014585.5:c.193G>C , LRG_837t1:c.193G>C NP_055400.1:p.Gly65Arg
XM_005246505.1:c.73G>C XP_005246562.1:p.Gly25Arg
XM_005246505.2:c.73G>C XP_005246562.1:p.Gly25Arg
XM_017003938.2:c.73G>C XP_016859427.1:p.Gly25Arg
NM_014585.6:c.193G>C MANE Select NP_055400.1:p.Gly65Arg
Search 100 bp 5'
Search 100 bp 3'