Canonical Allele Identifier: CA14218263

Gene: CTF2P

Linked Data

• dbSNP Id: rs1458201
• gnomAD v2: 16-30916129-G-A
• gnomAD v3: 16-30904808-G-A
• gnomAD v4: 16-30904808-G-A
• MyVariant Identifiers: chr16:g.30916129G>A (hg19) ; chr16:g.30904808G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30904808G>A , CM000678.2:g.30904808G>A	GRCh38
NC_000016.9:g.30916129G>A , CM000678.1:g.30916129G>A	GRCh37
NC_000016.8:g.30823630G>A	NCBI36
NG_009171.1:g.13202G>A , LRG_408:g.13202G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000412003.1:n.154-10C>T