Canonical Allele Identifier: CA7329594

Gene:

Linked Data

• dbSNP Id: rs1884082
• ExAC: 14:95078677 G / T
• gnomAD v2: 14-95078677-G-T
• gnomAD v3: 14-94612340-G-T
• gnomAD v4: 14-94612340-G-T
• MyVariant Identifiers: chr14:g.95078677G>T (hg19) ; chr14:g.94612340G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94612340G>T , CM000676.2:g.94612340G>T	GRCh38
NC_000014.8:g.95078677G>T , CM000676.1:g.95078677G>T	GRCh37
NC_000014.7:g.94148430G>T	NCBI36
NG_012879.1:g.4964G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553947.1:c.848G>T