Canonical Allele Identifier: CA151235372

Gene:

Linked Data

• dbSNP Id: rs752530100
• gnomAD v3: 6-160668583-C-G
• gnomAD v4: 6-160668583-C-G
• MyVariant Identifiers: chr6:g.161089615C>G (hg19) ; chr6:g.160668583C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668583C>G , CM000668.2:g.160668583C>G	GRCh38
NC_000006.11:g.161089615C>G , CM000668.1:g.161089615C>G	GRCh37
NC_000006.10:g.161009605C>G	NCBI36
NG_016147.1:g.2793G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2210G>C