Canonical Allele Identifier: CA349987166
Gene: SLC40A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.190428337A>C (hg19) chr2:g.189563611A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563611A>C , CM000664.2:g.189563611A>C GRCh38
NC_000002.11:g.190428337A>C , CM000664.1:g.190428337A>C GRCh37
NC_000002.10:g.190136582A>C NCBI36
NG_009027.1:g.22201T>G , LRG_837:g.22201T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1375T>G MANE Select ENSP00000261024.3:p.Phe459Val
ENST00000261024.6:c.1375T>G ENSP00000261024.2:p.Phe459Val
NM_014585.5:c.1375T>G , LRG_837t1:c.1375T>G NP_055400.1:p.Phe459Val
XM_005246505.1:c.1255T>G XP_005246562.1:p.Phe419Val
XM_005246505.2:c.1255T>G XP_005246562.1:p.Phe419Val
XM_017003938.2:c.1255T>G XP_016859427.1:p.Phe419Val
NM_014585.6:c.1375T>G MANE Select NP_055400.1:p.Phe459Val
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