Canonical Allele Identifier: CA2166464619
Gene: OCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28090600_28090601delinsCA , CM000677.2:g.28090600_28090601delinsCA GRCh38
NC_000015.9:g.28335746_28335747delinsCA , CM000677.1:g.28335746_28335747delinsCA GRCh37
NC_000015.8:g.26009341_26009342delinsCA NCBI36
NG_009846.1:g.13712_13713delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000354638.8:c.-22+8623_-22+8624delinsTG MANE Select ENSP00000346659.3:n.-22+8623_-22+8624deli...
ENST00000353809.9:c.-22+8623_-22+8624delinsTG ENSP00000261276.8:n.-22+8623_-22+8624deli...
ENST00000354638.7:c.-22+8623_-22+8624delinsTG ENSP00000346659.3:n.-22+8623_-22+8624deli...
ENST00000431101.1:c.-22+8510_-22+8511delinsTG ENSP00000415431.1:n.-22+8510_-22+8511deli...
ENST00000445578.5:c.-22+8623_-22+8624delinsTG ENSP00000414425.1:n.-22+8623_-22+8624deli...
NM_000275.2:c.-22+8623_-22+8624delinsTG NP_000266.2:n.-22+8623_-22+8624delinsTG
NM_001300984.1:c.-22+8623_-22+8624delinsTG NP_001287913.1:n.-22+8623_-22+8624delinsT...
XM_011521640.1:c.-22+8623_-22+8624delinsTG XP_011519942.1:n.-22+8623_-22+8624delinsT...
XM_011521640.2:c.-22+8623_-22+8624delinsTG XP_011519942.1:n.-22+8623_-22+8624delinsT...
NM_000275.3:c.-22+8623_-22+8624delinsTG MANE Select NP_000266.2:n.-22+8623_-22+8624delinsTG
NM_001300984.2:c.-22+8623_-22+8624delinsTG NP_001287913.1:n.-22+8623_-22+8624delinsT...