Canonical Allele Identifier: CA726478698
Gene: TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1373473346
gnomAD v3: 17-15999790-G-C
gnomAD v4: 17-15999790-G-C
MyVariant Identifiers: chr17:g.15903104G>C (hg19) chr17:g.15999790G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999790G>C , CM000679.2:g.15999790G>C GRCh38
NC_000017.10:g.15903104G>C , CM000679.1:g.15903104G>C GRCh37
NC_000017.9:g.15843829G>C NCBI36
NG_029806.1:g.5411G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-59G>C ENSP00000261647.5:n.-59G>C
ENST00000466729.5:c.7G>C
NM_001271420.1:c.-517G>C NP_001258349.1:n.-517G>C
NM_017775.3:c.-59G>C NP_060245.3:n.-59G>C
XM_011523950.1:c.-59G>C XP_011522252.1:n.-59G>C
XM_017024801.2:c.-59G>C XP_016880290.2:n.-59G>C
XM_017024802.2:c.-59G>C XP_016880291.2:n.-59G>C
XM_024450814.1:c.-59G>C XP_024306582.1:n.-59G>C
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