Canonical Allele Identifier: CA508089531
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060860-A-G
MyVariant Identifiers: chr19:g.49564117A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060860A>G , CM000681.2:g.49060860A>G GRCh38
NC_000019.9:g.49564117A>G , CM000681.1:g.49564117A>G GRCh37
NC_000019.8:g.54255929A>G NCBI36
NG_016289.1:g.8008T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+895T>C ENSP00000470689.1:n.243+895T>C
XM_011527575.1:c.-108T>C XP_011525877.1:n.-108T>C
XR_001753693.1:n.879+304T>C
XR_001753694.1:n.880-51T>C
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