Canonical Allele Identifier: CA571118995

Gene:

Linked Data

• dbSNP Id: rs77275268
• gnomAD v2: 6-151969198-C-A
• gnomAD v3: 6-151648063-C-A
• gnomAD v4: 6-151648063-C-A
• MyVariant Identifiers: chr6:g.151969198C>A (hg19) ; chr6:g.151648063C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151648063C>A , CM000668.2:g.151648063C>A	GRCh38
NC_000006.11:g.151969198C>A , CM000668.1:g.151969198C>A	GRCh37
NC_000006.10:g.152010891C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2497-3634C>A