Canonical Allele Identifier: CA508089878
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060961-T-C
MyVariant Identifiers: chr19:g.49564218T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060961T>C , CM000681.2:g.49060961T>C GRCh38
NC_000019.9:g.49564218T>C , CM000681.1:g.49564218T>C GRCh37
NC_000019.8:g.54256030T>C NCBI36
NG_016289.1:g.7907A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+794A>G ENSP00000470689.1:n.243+794A>G
XM_011527575.1:c.-209A>G XP_011525877.1:n.-209A>G
XR_001753693.1:n.879+203A>G
XR_001753694.1:n.880-152A>G
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