Canonical Allele Identifier: CA151235339

Gene:

Linked Data

• dbSNP Id: rs974494244
• MyVariant Identifiers: chr6:g.161089554G>A (hg19) ; chr6:g.160668522G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668522G>A , CM000668.2:g.160668522G>A	GRCh38
NC_000006.11:g.161089554G>A , CM000668.1:g.161089554G>A	GRCh37
NC_000006.10:g.161009544G>A	NCBI36
NG_016147.1:g.2854C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2149C>T