Canonical Allele Identifier: CA508089742
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564182C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060925C>G , CM000681.2:g.49060925C>G GRCh38
NC_000019.9:g.49564182C>G , CM000681.1:g.49564182C>G GRCh37
NC_000019.8:g.54255994C>G NCBI36
NG_016289.1:g.7943G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+830G>C ENSP00000470689.1:n.243+830G>C
XM_011527575.1:c.-173G>C XP_011525877.1:n.-173G>C
XR_001753693.1:n.879+239G>C
XR_001753694.1:n.880-116G>C
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