Canonical Allele Identifier: CA150162913

Gene:

Linked Data

• dbSNP Id: rs1006765483
• MyVariant Identifiers: chr6:g.151954751C>A (hg19) ; chr6:g.151633616C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633616C>A , CM000668.2:g.151633616C>A	GRCh38
NC_000006.11:g.151954751C>A , CM000668.1:g.151954751C>A	GRCh37
NC_000006.10:g.151996444C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3634C>A