Canonical Allele Identifier: CA508089121
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs908519250
MyVariant Identifiers: chr19:g.49563989G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060732G>C , CM000681.2:g.49060732G>C GRCh38
NC_000019.9:g.49563989G>C , CM000681.1:g.49563989G>C GRCh37
NC_000019.8:g.54255801G>C NCBI36
NG_016289.1:g.8136C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+1023C>G ENSP00000470689.1:n.243+1023C>G
XM_011527575.1:c.21C>G XP_011525877.1:p.Leu7=
XR_001753693.1:n.879+432C>G
XR_001753694.1:n.957C>G
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