Canonical Allele Identifier: CA261711536

Gene:

Linked Data

• dbSNP Id: rs767603
• gnomAD v2: 14-61098683-T-C
• gnomAD v3: 14-60631965-T-C
• gnomAD v4: 14-60631965-T-C
• MyVariant Identifiers: chr14:g.61098683T>C (hg19) ; chr14:g.60631965T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60631965T>C , CM000676.2:g.60631965T>C	GRCh38
NC_000014.8:g.61098683T>C , CM000676.1:g.61098683T>C	GRCh37
NC_000014.7:g.60168436T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537451.1:c.1201+9598A>G	XP_011535753.1:n.1201+9598A>G
XM_011537451.3:c.1201+9598A>G	XP_011535753.1:n.1201+9598A>G