Canonical Allele Identifier: CA151235369

Gene:

Linked Data

• dbSNP Id: rs776189249
• MyVariant Identifiers: chr6:g.161089593C>A (hg19) ; chr6:g.160668561C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668561C>A , CM000668.2:g.160668561C>A	GRCh38
NC_000006.11:g.161089593C>A , CM000668.1:g.161089593C>A	GRCh37
NC_000006.10:g.161009583C>A	NCBI36
NG_016147.1:g.2815G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2188G>T