Canonical Allele Identifier: CA7329602

Gene:

Linked Data

• dbSNP Id: rs745574605
• ExAC: 14:95078685 G / T
• gnomAD v2: 14-95078685-G-T
• gnomAD v4: 14-94612348-G-T
• MyVariant Identifiers: chr14:g.95078685G>T (hg19) ; chr14:g.94612348G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94612348G>T , CM000676.2:g.94612348G>T	GRCh38
NC_000014.8:g.95078685G>T , CM000676.1:g.95078685G>T	GRCh37
NC_000014.7:g.94148438G>T	NCBI36
NG_012879.1:g.4972G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553947.1:c.856G>T