Canonical Allele Identifier: CA1315653403
Gene: SLC40A1 HGNC NCBI

Linked Data

dbSNP Id: rs1473801584
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575006T>C , CM000664.2:g.189575006T>C GRCh38
NC_000002.11:g.190439732T>C , CM000664.1:g.190439732T>C GRCh37
NC_000002.10:g.190147977T>C NCBI36
NG_009027.1:g.10806A>G , LRG_837:g.10806A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.271+155A>G MANE Select ENSP00000261024.3:n.271+155A>G
ENST00000261024.6:c.271+155A>G ENSP00000261024.2:n.271+155A>G
ENST00000427241.5:c.271+155A>G ENSP00000390005.1:n.271+155A>G
ENST00000479598.5:n.552+155A>G
NM_014585.5:c.271+155A>G , LRG_837t1:c.271+155A>G NP_055400.1:n.271+155A>G
XM_005246505.1:c.151+155A>G XP_005246562.1:n.151+155A>G
XM_005246505.2:c.151+155A>G XP_005246562.1:n.151+155A>G
XM_017003938.2:c.151+155A>G XP_016859427.1:n.151+155A>G
NM_014585.6:c.271+155A>G MANE Select NP_055400.1:n.271+155A>G
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