Canonical Allele Identifier: CA508089305
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs2040121864
MyVariant Identifiers: chr19:g.49564046C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060789C>A , CM000681.2:g.49060789C>A GRCh38
NC_000019.9:g.49564046C>A , CM000681.1:g.49564046C>A GRCh37
NC_000019.8:g.54255858C>A NCBI36
NG_016289.1:g.8079G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000599795.5:c.243+966G>T ENSP00000470689.1:n.243+966G>T
XM_011527575.1:c.-37G>T XP_011525877.1:n.-37G>T
XR_001753693.1:n.879+375G>T
XR_001753694.1:n.900G>T
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