Canonical Allele Identifier: CA2739521151
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999804C>G , CM000679.2:g.15999804C>G GRCh38
NC_000017.10:g.15903118C>G , CM000679.1:g.15903118C>G GRCh37
NC_000017.9:g.15843843C>G NCBI36
NG_029806.1:g.5425C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-45C>G ENSP00000261647.5:n.-45C>G
ENST00000466729.5:c.21C>G
ENST00000475723.5:c.3C>G
NM_001271420.1:c.-503C>G NP_001258349.1:n.-503C>G
NM_017775.3:c.-45C>G NP_060245.3:n.-45C>G
XM_011523950.1:c.-45C>G XP_011522252.1:n.-45C>G
XM_017024801.2:c.-45C>G XP_016880290.2:n.-45C>G
XM_017024802.2:c.-45C>G XP_016880291.2:n.-45C>G
XM_024450814.1:c.-45C>G XP_024306582.1:n.-45C>G