Canonical Allele Identifier: CA2024139
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2897466
ClinVar RCV Id: RCV003615245
dbSNP Id: rs763703768
ExAC: 2:190428866 A / G
gnomAD v2: 2-190428866-A-G
gnomAD v4: 2-189564140-A-G
MyVariant Identifiers: chr2:g.190428866A>G (hg19) chr2:g.189564140A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564140A>G , CM000664.2:g.189564140A>G GRCh38
NC_000002.11:g.190428866A>G , CM000664.1:g.190428866A>G GRCh37
NC_000002.10:g.190137111A>G NCBI36
NG_009027.1:g.21672T>C , LRG_837:g.21672T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.846T>C MANE Select ENSP00000261024.3:p.Pro282=
ENST00000261024.6:c.846T>C ENSP00000261024.2:p.Pro282=
NM_014585.5:c.846T>C , LRG_837t1:c.846T>C NP_055400.1:p.Pro282=
XM_005246505.1:c.726T>C XP_005246562.1:p.Pro242=
XM_005246505.2:c.726T>C XP_005246562.1:p.Pro242=
XM_017003938.2:c.726T>C XP_016859427.1:p.Pro242=
NM_014585.6:c.846T>C MANE Select NP_055400.1:p.Pro282=
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