Canonical Allele Identifier: CA678988243
Gene: BEST1 HGNC NCBI

Linked Data

dbSNP Id: rs1479030247

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61950403A>G , CM000673.2:g.61950403A>G GRCh38
NC_000011.9:g.61717875A>G , CM000673.1:g.61717875A>G GRCh37
NC_000011.8:g.61474451A>G NCBI36
NG_009033.1:g.5520A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.-61A>G MANE Select ENSP00000367282.4:n.-61A>G
ENST00000378043.8:c.-61A>G ENSP00000367282.4:n.-61A>G
ENST00000449131.6:c.-53A>G ENSP00000399709.2:n.-53A>G
ENST00000524877.5:n.44A>G
ENST00000524926.5:c.-61A>G ENSP00000432681.1:n.-61A>G
ENST00000529265.5:n.51A>G
ENST00000533521.5:n.48A>G
ENST00000534553.5:c.-236A>G ENSP00000431189.1:n.-236A>G
NM_001139443.1:c.-53A>G NP_001132915.1:n.-53A>G
NM_001300786.1:c.-53A>G NP_001287715.1:n.-53A>G
NM_001300787.1:c.-53A>G NP_001287716.1:n.-53A>G
NM_004183.3:c.-61A>G NP_004174.1:n.-61A>G
XM_005274210.2:c.-61A>G XP_005274267.1:n.-61A>G
XM_005274216.2:c.-53A>G XP_005274273.1:n.-53A>G
XM_005274218.3:c.-236A>G XP_005274275.1:n.-236A>G
XM_005274219.2:c.-61A>G XP_005274276.1:n.-61A>G
XM_005274221.2:c.-61A>G XP_005274278.1:n.-61A>G
XM_011545229.1:c.-36-1368A>G XP_011543531.1:n.-36-1368A>G
XM_011545230.1:c.59+3588A>G XP_011543532.1:n.59+3588A>G
XM_011545231.1:c.-236A>G XP_011543533.1:n.-236A>G
XM_011545232.1:c.-61A>G XP_011543534.1:n.-61A>G
NM_001363592.1:c.-61A>G NP_001350521.1:n.-61A>G
NR_134580.1:n.520A>G
XM_005274210.4:c.-61A>G XP_005274267.1:n.-61A>G
XM_005274216.4:c.-53A>G XP_005274273.1:n.-53A>G
XM_005274219.4:c.-61A>G XP_005274276.1:n.-61A>G
XM_005274221.4:c.-61A>G XP_005274278.1:n.-61A>G
XM_011545229.3:c.-36-1368A>G XP_011543531.1:n.-36-1368A>G
XM_011545230.3:c.59+3588A>G XP_011543532.1:n.59+3588A>G
XR_001747952.2:n.626A>G
XR_001747953.2:n.630A>G
XR_001747954.2:n.630A>G
NM_004183.4:c.-61A>G MANE Select NP_004174.1:n.-61A>G
NM_001139443.2:c.-53A>G NP_001132915.1:n.-53A>G
NM_001300786.2:c.-53A>G NP_001287715.1:n.-53A>G
NM_001300787.2:c.-53A>G NP_001287716.1:n.-53A>G
NR_134580.2:n.53A>G