Canonical Allele Identifier: CA508089830

Gene: NTF4

Linked Data

• gnomAD v4: 19-49060950-A-C
• MyVariant Identifiers: chr19:g.49564207A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060950A>C , CM000681.2:g.49060950A>C	GRCh38
NC_000019.9:g.49564207A>C , CM000681.1:g.49564207A>C	GRCh37
NC_000019.8:g.54256019A>C	NCBI36
NG_016289.1:g.7918T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+805T>G	ENSP00000470689.1:n.243+805T>G
XM_011527575.1:c.-198T>G	XP_011525877.1:n.-198T>G
XR_001753693.1:n.879+214T>G
XR_001753694.1:n.880-141T>G