Canonical Allele Identifier: CA508090208
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564309C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061052C>G , CM000681.2:g.49061052C>G GRCh38
NC_000019.9:g.49564309C>G , CM000681.1:g.49564309C>G GRCh37
NC_000019.8:g.54256121C>G NCBI36
NG_016289.1:g.7816G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+703G>C ENSP00000470689.1:n.243+703G>C
XR_001753693.1:n.879+112G>C
XR_001753694.1:n.879+112G>C
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