Canonical Allele Identifier: CA508089796
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1327664596
gnomAD v3: 19-49060939-T-C
gnomAD v4: 19-49060939-T-C
MyVariant Identifiers: chr19:g.49564196T>C (hg19) chr19:g.49060939T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060939T>C , CM000681.2:g.49060939T>C GRCh38
NC_000019.9:g.49564196T>C , CM000681.1:g.49564196T>C GRCh37
NC_000019.8:g.54256008T>C NCBI36
NG_016289.1:g.7929A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+816A>G ENSP00000470689.1:n.243+816A>G
XM_011527575.1:c.-187A>G XP_011525877.1:n.-187A>G
XR_001753693.1:n.879+225A>G
XR_001753694.1:n.880-130A>G
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