Canonical Allele Identifier: CA508089677

Gene: NTF4

Linked Data

• dbSNP Id: rs1342716108
• gnomAD v2: 19-49564163-G-A
• gnomAD v3: 19-49060906-G-A
• gnomAD v4: 19-49060906-G-A
• MyVariant Identifiers: chr19:g.49564163G>A (hg19) ; chr19:g.49060906G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060906G>A , CM000681.2:g.49060906G>A	GRCh38
NC_000019.9:g.49564163G>A , CM000681.1:g.49564163G>A	GRCh37
NC_000019.8:g.54255975G>A	NCBI36
NG_016289.1:g.7962C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+849C>T	ENSP00000470689.1:n.243+849C>T
XM_011527575.1:c.-154C>T	XP_011525877.1:n.-154C>T
XR_001753693.1:n.879+258C>T
XR_001753694.1:n.880-97C>T