Allele Registry

Canonical Allele Identifier: CA525390634

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.113761214T>G

GRCh37 chr1:g.114303836T>G

Linked Data - Sequence & Population

gnomAD v2:

1:114303836 T / G

gnomAD v3:

1:113761214 T / G

gnomAD v4:

chr1-113761214-T-G

Linked Data - NCBI & NCI

dbSNP:

1236054095

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113761214T>G , CM000663.2:g.113761214T>G	GRCh38
NC_000001.10:g.114303836T>G , CM000663.1:g.114303836T>G	GRCh37
NC_000001.9:g.114105359T>G	NCBI36

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