Canonical Allele Identifier: CA150162784

Gene:

Linked Data

• dbSNP Id: rs868171853
• gnomAD v2: 6-151954552-G-A
• gnomAD v3: 6-151633417-G-A
• gnomAD v4: 6-151633417-G-A
• MyVariant Identifiers: chr6:g.151954552G>A (hg19) ; chr6:g.151633417G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633417G>A , CM000668.2:g.151633417G>A	GRCh38
NC_000006.11:g.151954552G>A , CM000668.1:g.151954552G>A	GRCh37
NC_000006.10:g.151996245G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3435G>A