Canonical Allele Identifier: CA222930138
Gene: BEST1 HGNC NCBI

Linked Data

dbSNP Id: rs950317499

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61950368C>T , CM000673.2:g.61950368C>T GRCh38
NC_000011.9:g.61717840C>T , CM000673.1:g.61717840C>T GRCh37
NC_000011.8:g.61474416C>T NCBI36
NG_009033.1:g.5485C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.-96C>T MANE Select ENSP00000367282.4:n.-96C>T
ENST00000378043.8:c.-96C>T ENSP00000367282.4:n.-96C>T
ENST00000524877.5:n.9C>T
ENST00000524926.5:c.-96C>T ENSP00000432681.1:n.-96C>T
ENST00000529265.5:n.16C>T
ENST00000533521.5:n.13C>T
ENST00000534553.5:c.-271C>T ENSP00000431189.1:n.-271C>T
NM_001139443.1:c.-88C>T NP_001132915.1:n.-88C>T
NM_001300786.1:c.-88C>T NP_001287715.1:n.-88C>T
NM_001300787.1:c.-88C>T NP_001287716.1:n.-88C>T
NM_004183.3:c.-96C>T NP_004174.1:n.-96C>T
XM_005274210.2:c.-96C>T XP_005274267.1:n.-96C>T
XM_005274216.2:c.-88C>T XP_005274273.1:n.-88C>T
XM_005274218.3:c.-271C>T XP_005274275.1:n.-271C>T
XM_005274219.2:c.-96C>T XP_005274276.1:n.-96C>T
XM_005274221.2:c.-96C>T XP_005274278.1:n.-96C>T
XM_011545229.1:c.-36-1403C>T XP_011543531.1:n.-36-1403C>T
XM_011545230.1:c.59+3553C>T XP_011543532.1:n.59+3553C>T
XM_011545231.1:c.-271C>T XP_011543533.1:n.-271C>T
XM_011545232.1:c.-96C>T XP_011543534.1:n.-96C>T
NM_001363592.1:c.-96C>T NP_001350521.1:n.-96C>T
NR_134580.1:n.485C>T
XM_005274210.4:c.-96C>T XP_005274267.1:n.-96C>T
XM_005274216.4:c.-88C>T XP_005274273.1:n.-88C>T
XM_005274219.4:c.-96C>T XP_005274276.1:n.-96C>T
XM_005274221.4:c.-96C>T XP_005274278.1:n.-96C>T
XM_011545229.3:c.-36-1403C>T XP_011543531.1:n.-36-1403C>T
XM_011545230.3:c.59+3553C>T XP_011543532.1:n.59+3553C>T
XR_001747952.2:n.591C>T
XR_001747953.2:n.595C>T
XR_001747954.2:n.595C>T
NM_004183.4:c.-96C>T MANE Select NP_004174.1:n.-96C>T
NM_001139443.2:c.-88C>T NP_001132915.1:n.-88C>T
NM_001300786.2:c.-88C>T NP_001287715.1:n.-88C>T
NM_001300787.2:c.-88C>T NP_001287716.1:n.-88C>T
NR_134580.2:n.18C>T