Canonical Allele Identifier: CA151235612

Gene:

Linked Data

• dbSNP Id: rs201168950
• gnomAD v2: 6-161089833-T-C
• gnomAD v3: 6-160668801-T-C
• gnomAD v4: 6-160668801-T-C
• COSMIC: COSN19686176
• MyVariant Identifiers: chr6:g.161089833T>C (hg19) ; chr6:g.161089833_161089838delinsCTATCA (hg19) ; chr6:g.160668801T>C (hg38) ; chr6:g.160668801_160668806delinsCTATCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668801T>C , CM000668.2:g.160668801T>C	GRCh38
NC_000006.11:g.161089833T>C , CM000668.1:g.161089833T>C	GRCh37
NC_000006.10:g.161009823T>C	NCBI36
NG_016147.1:g.2575A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2428A>G