Canonical Allele Identifier: CA150162802

Gene:

Linked Data

• dbSNP Id: rs980318597
• gnomAD v2: 6-151954597-G-A
• MyVariant Identifiers: chr6:g.151954597G>A (hg19) ; chr6:g.151633462G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633462G>A , CM000668.2:g.151633462G>A	GRCh38
NC_000006.11:g.151954597G>A , CM000668.1:g.151954597G>A	GRCh37
NC_000006.10:g.151996290G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3480G>A