Canonical Allele Identifier: CA26899192

Gene:

Linked Data

• dbSNP Id: rs767171804
• gnomAD v3: 1-94564051-T-C
• gnomAD v4: 1-94564051-T-C
• MyVariant Identifiers: chr1:g.95029607T>C (hg19) ; chr1:g.94564051T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94564051T>C , CM000663.2:g.94564051T>C	GRCh38
NC_000001.10:g.95029607T>C , CM000663.1:g.95029607T>C	GRCh37
NC_000001.9:g.94802195T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001738161.1:n.461+438T>C