Canonical Allele Identifier: CA2156070669

Gene:

Linked Data

• dbSNP Id: rs1885810912
• gnomAD v4: 14-94612353-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94612353C>T , CM000676.2:g.94612353C>T	GRCh38
NC_000014.8:g.95078690C>T , CM000676.1:g.95078690C>T	GRCh37
NC_000014.7:g.94148443C>T	NCBI36
NG_012879.1:g.4977C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553947.1:c.861C>T