Canonical Allele Identifier: CA35603697

Gene:

Linked Data

• dbSNP Id: rs114652390
• gnomAD v2: 1-202909068-A-C
• gnomAD v3: 1-202939940-A-C
• gnomAD v4: 1-202939940-A-C
• MyVariant Identifiers: chr1:g.202909068A>C (hg19) ; chr1:g.202909068_202909071delinsCCTT (hg19) ; chr1:g.202939940A>C (hg38) ; chr1:g.202939940_202939943delinsCCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202939940A>C , CM000663.2:g.202939940A>C	GRCh38
NC_000001.10:g.202909068A>C , CM000663.1:g.202909068A>C	GRCh37
NC_000001.9:g.201175691A>C	NCBI36
NG_052860.1:g.23633T>G