Canonical Allele Identifier: CA151235332

Gene:

Linked Data

• dbSNP Id: rs964138691
• MyVariant Identifiers: chr6:g.161089538C>T (hg19) ; chr6:g.160668506C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668506C>T , CM000668.2:g.160668506C>T	GRCh38
NC_000006.11:g.161089538C>T , CM000668.1:g.161089538C>T	GRCh37
NC_000006.10:g.161009528C>T	NCBI36
NG_016147.1:g.2870G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2133G>A