Canonical Allele Identifier: CA508089631

Gene: NTF4

Linked Data

• dbSNP Id: rs1359952562
• gnomAD v2: 19-49564150-A-C
• gnomAD v3: 19-49060893-A-C
• gnomAD v4: 19-49060893-A-C
• MyVariant Identifiers: chr19:g.49564150A>C (hg19) ; chr19:g.49060893A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060893A>C , CM000681.2:g.49060893A>C	GRCh38
NC_000019.9:g.49564150A>C , CM000681.1:g.49564150A>C	GRCh37
NC_000019.8:g.54255962A>C	NCBI36
NG_016289.1:g.7975T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+862T>G	ENSP00000470689.1:n.243+862T>G
XM_011527575.1:c.-141T>G	XP_011525877.1:n.-141T>G
XR_001753693.1:n.879+271T>G
XR_001753694.1:n.880-84T>G