Canonical Allele Identifier: CA15836280

Gene: SNHG14

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.24990569G>A , CM000677.2:g.24990569G>A	GRCh38
NC_000015.9:g.25235716G>A , CM000677.1:g.25235716G>A	GRCh37
NC_000015.8:g.22786809G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551312.6:c.*953+8132G>A	ENSP00000451421.1:n.*953+8132G>A
ENST00000557230.1:c.*400-8401G>A	ENSP00000451898.1:n.*400-8401G>A
NR_146177.1:n.3625-7797G>A