Canonical Allele Identifier: CA2613918997

Gene: BEST1

Linked Data

• gnomAD v4: 11-61950276-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61950276T>C , CM000673.2:g.61950276T>C	GRCh38
NC_000011.9:g.61717748T>C , CM000673.1:g.61717748T>C	GRCh37
NC_000011.8:g.61474324T>C	NCBI36
NG_009033.1:g.5393T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.8:c.-188T>C	ENSP00000367282.4:n.-188T>C
ENST00000534553.5:c.-363T>C	ENSP00000431189.1:n.-363T>C
NM_001139443.1:c.-180T>C	NP_001132915.1:n.-180T>C
NM_001300786.1:c.-180T>C	NP_001287715.1:n.-180T>C
NM_001300787.1:c.-180T>C	NP_001287716.1:n.-180T>C
NM_004183.3:c.-188T>C	NP_004174.1:n.-188T>C
XM_005274210.2:c.-188T>C	XP_005274267.1:n.-188T>C
XM_005274216.2:c.-180T>C	XP_005274273.1:n.-180T>C
XM_005274218.3:c.-363T>C	XP_005274275.1:n.-363T>C
XM_005274219.2:c.-188T>C	XP_005274276.1:n.-188T>C
XM_005274221.2:c.-188T>C	XP_005274278.1:n.-188T>C
XM_011545229.1:c.-36-1495T>C	XP_011543531.1:n.-36-1495T>C
XM_011545230.1:c.59+3461T>C	XP_011543532.1:n.59+3461T>C
XM_011545231.1:c.-363T>C	XP_011543533.1:n.-363T>C
XM_011545232.1:c.-188T>C	XP_011543534.1:n.-188T>C
NM_001363592.1:c.-188T>C	NP_001350521.1:n.-188T>C
NR_134580.1:n.393T>C
XM_005274210.4:c.-188T>C	XP_005274267.1:n.-188T>C
XM_005274216.4:c.-180T>C	XP_005274273.1:n.-180T>C
XM_005274219.4:c.-188T>C	XP_005274276.1:n.-188T>C
XM_005274221.4:c.-188T>C	XP_005274278.1:n.-188T>C
XM_011545229.3:c.-36-1495T>C	XP_011543531.1:n.-36-1495T>C
XM_011545230.3:c.59+3461T>C	XP_011543532.1:n.59+3461T>C
XR_001747952.2:n.499T>C
XR_001747953.2:n.503T>C
XR_001747954.2:n.503T>C