Canonical Allele Identifier: CA2685597805
Gene: AOC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150861300C>T , CM000669.2:g.150861300C>T GRCh38
NC_000007.13:g.150558388C>T , CM000669.1:g.150558388C>T GRCh37
NC_000007.12:g.150189321C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.*91C>T MANE Select ENSP00000354193.4:n.*91C>T
ENST00000360937.8:c.*91C>T ENSP00000354193.4:n.*91C>T
ENST00000467291.5:c.*91C>T ENSP00000418328.1:n.*91C>T
ENST00000493429.5:c.*91C>T ENSP00000418614.1:n.*91C>T
XR_928169.1:n.295+15709G>A
XR_928170.1:n.425+7316G>A
XR_928171.1:n.297+15709G>A
XR_928169.2:n.301+15709G>A
XR_928171.2:n.301+15709G>A
NM_001091.4:c.*91C>T MANE Select NP_001082.2:n.*91C>T
NM_001272072.2:c.*91C>T NP_001259001.1:n.*91C>T