Allele Registry

Canonical Allele Identifier: CA191124909

Gene: SLC24A2 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.20145990T>C

GRCh37 chr9:g.20145988T>C

Linked Data - Sequence & Population

gnomAD v2:

9:20145988 T / C

gnomAD v3:

9:20145990 T / C

gnomAD v4:

chr9-20145990-T-C

Joint Max Group AF 0.6249196 (NFE)

Genomes Max Group AF 0.6249196 (NFE)

Linked Data - NCBI & NCI

dbSNP:

2039461

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.20145990T>C , CM000671.2:g.20145990T>C	GRCh38
NC_000009.11:g.20145988T>C , CM000671.1:g.20145988T>C	GRCh37
NC_000009.10:g.20135988T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017014592.1:c.-528-141603A>G	XP_016870081.1:n.-528-141603A>G

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