Canonical Allele Identifier: CA151235192

Gene:

Linked Data

• dbSNP Id: rs1003374903
• MyVariant Identifiers: chr6:g.161089453G>C (hg19) ; chr6:g.160668421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160668421G>C , CM000668.2:g.160668421G>C	GRCh38
NC_000006.11:g.161089453G>C , CM000668.1:g.161089453G>C	GRCh37
NC_000006.10:g.161009443G>C	NCBI36
NG_016147.1:g.2955C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452651.1:n.115-2048C>G