Canonical Allele Identifier: CA670191438

Gene:

Linked Data

• dbSNP Id: rs1162541858
• gnomAD v3: 10-94762614-T-G
• gnomAD v4: 10-94762614-T-G
• MyVariant Identifiers: chr10:g.96522371T>G (hg19) ; chr10:g.94762614T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762614T>G , CM000672.2:g.94762614T>G	GRCh38
NC_000010.10:g.96522371T>G , CM000672.1:g.96522371T>G	GRCh37
NC_000010.9:g.96512361T>G	NCBI36
NG_008384.2:g.4909T>G
NG_008384.3:g.4934T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000464755.1:c.932-12444T>G	ENSP00000483243.1:n.932-12444T>G