Canonical Allele Identifier: CA7329599

Gene:

Linked Data

• dbSNP Id: rs746778017
• ExAC: 14:95078683 G / T
• gnomAD v2: 14-95078683-G-T
• gnomAD v4: 14-94612346-G-T
• MyVariant Identifiers: chr14:g.95078683G>T (hg19) ; chr14:g.94612346G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94612346G>T , CM000676.2:g.94612346G>T	GRCh38
NC_000014.8:g.95078683G>T , CM000676.1:g.95078683G>T	GRCh37
NC_000014.7:g.94148436G>T	NCBI36
NG_012879.1:g.4970G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553947.1:c.854G>T