Allele Registry

Canonical Allele Identifier: CA14241441

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr16:g.13882499T>C

GRCh37 chr16:g.13976356T>C

Linked Data - Sequence & Population

gnomAD v2:

16:13976356 T / C

gnomAD v3:

16:13882499 T / C

gnomAD v4:

chr16-13882499-T-C

Joint Max Group AF 0.75890286 (NFE)

Genomes Max Group AF 0.75890286 (NFE)

Linked Data - NCBI & NCI

dbSNP:

2113334

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13882499T>C , CM000678.2:g.13882499T>C	GRCh38
NC_000016.9:g.13976356T>C , CM000678.1:g.13976356T>C	GRCh37
NC_000016.8:g.13883857T>C	NCBI36

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