Canonical Allele Identifier: CA570684213

Gene:

Linked Data

• dbSNP Id: rs1359405742
• gnomAD v2: 6-134720030-G-A
• gnomAD v3: 6-134398892-G-A
• gnomAD v4: 6-134398892-G-A
• MyVariant Identifiers: chr6:g.134720030G>A (hg19) ; chr6:g.134398892G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.134398892G>A , CM000668.2:g.134398892G>A	GRCh38
NC_000006.11:g.134720030G>A , CM000668.1:g.134720030G>A	GRCh37
NC_000006.10:g.134761723G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428023.2:n.23+163G>A