Canonical Allele Identifier: CA624961133
Gene: TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1364516857
gnomAD v2: 17-15903066-C-T
gnomAD v4: 17-15999752-C-T
MyVariant Identifiers: chr17:g.15903066C>T (hg19) chr17:g.15999752C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999752C>T , CM000679.2:g.15999752C>T GRCh38
NC_000017.10:g.15903066C>T , CM000679.1:g.15903066C>T GRCh37
NC_000017.9:g.15843791C>T NCBI36
NG_029806.1:g.5373C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-97C>T ENSP00000261647.5:n.-97C>T
NM_001271420.1:c.-555C>T NP_001258349.1:n.-555C>T
NM_017775.3:c.-97C>T NP_060245.3:n.-97C>T
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