Canonical Allele Identifier: CA2636259650
Gene: TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-15999821-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999821T>C , CM000679.2:g.15999821T>C GRCh38
NC_000017.10:g.15903135T>C , CM000679.1:g.15903135T>C GRCh37
NC_000017.9:g.15843860T>C NCBI36
NG_029806.1:g.5442T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-28T>C ENSP00000261647.5:n.-28T>C
ENST00000466729.5:c.38T>C
ENST00000475723.5:c.20T>C
NM_001271420.1:c.-486T>C NP_001258349.1:n.-486T>C
NM_017775.3:c.-28T>C NP_060245.3:n.-28T>C
XM_011523950.1:c.-28T>C XP_011522252.1:n.-28T>C
XM_017024801.2:c.-28T>C XP_016880290.2:n.-28T>C
XM_017024802.2:c.-28T>C XP_016880291.2:n.-28T>C
XM_024450814.1:c.-28T>C XP_024306582.1:n.-28T>C
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