Canonical Allele Identifier: CA151235183

Gene:

Linked Data

• dbSNP Id: rs930519857
• gnomAD v3: 6-160668384-T-C
• gnomAD v4: 6-160668384-T-C
• MyVariant Identifiers: chr6:g.161089416T>C (hg19) ; chr6:g.160668384T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668384T>C , CM000668.2:g.160668384T>C	GRCh38
NC_000006.11:g.161089416T>C , CM000668.1:g.161089416T>C	GRCh37
NC_000006.10:g.161009406T>C	NCBI36
NG_016147.1:g.2992A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2011A>G