Canonical Allele Identifier: CA997753000

Gene:

Linked Data

• dbSNP Id: rs1659179201
• gnomAD v3: 1-2036364-T-G
• gnomAD v4: 1-2036364-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2036364T>G , CM000663.2:g.2036364T>G	GRCh38
NC_000001.10:g.1967803T>G , CM000663.1:g.1967803T>G	GRCh37
NC_000001.9:g.1957663T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946823.1:n.773+71A>C
XR_001737845.2:n.847A>C
XR_946823.3:n.776+71A>C