Canonical Allele Identifier: CA451072869

Gene: BCKDHB

Linked Data

• MyVariant Identifiers: chr6:g.80878714T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168997T>C , CM000668.2:g.80168997T>C	GRCh38
NC_000006.11:g.80878714T>C , CM000668.1:g.80878714T>C	GRCh37
NC_000006.10:g.80935433T>C	NCBI36
NG_009775.1:g.67371T>C
NG_009775.2:g.67371T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.600T>C MANE Select	ENSP00000318351.5:p.Pro200=
ENST00000320393.8:c.600T>C	ENSP00000318351.5:p.Pro200=
ENST00000356489.9:c.600T>C	ENSP00000348880.5:p.Pro200=
ENST00000369760.8:c.600T>C	ENSP00000358775.4:p.Pro200=
NM_000056.3:c.600T>C	NP_000047.1:p.Pro200=
NM_183050.2:c.600T>C	NP_898871.1:p.Pro200=
XM_005248756.3:c.600T>C	XP_005248813.1:p.Pro200=
XM_006715542.2:c.390T>C	XP_006715605.1:p.Pro130=
XM_011536023.1:c.600T>C	XP_011534325.1:p.Pro200=
XM_011536024.1:c.600T>C	XP_011534326.1:p.Pro200=
XM_011536025.1:c.600T>C	XP_011534327.1:p.Pro200=
XM_011536026.1:c.390T>C	XP_011534328.1:p.Pro130=
XM_011536027.1:c.600T>C	XP_011534329.1:p.Pro200=
NM_000056.4:c.600T>C	NP_000047.1:p.Pro200=
NM_001318975.1:c.390T>C	NP_001305904.1:p.Pro130=
NM_183050.3:c.600T>C	NP_898871.1:p.Pro200=
NR_134945.1:n.684T>C
XM_005248756.5:c.600T>C	XP_005248813.1:p.Pro200=
XM_011536023.3:c.600T>C	XP_011534325.1:p.Pro200=
XM_011536024.3:c.600T>C	XP_011534326.1:p.Pro200=
XM_011536025.3:c.600T>C	XP_011534327.1:p.Pro200=
XR_001743546.2:n.630T>C
XR_001743547.2:n.630T>C
XR_001743548.2:n.630T>C
XR_001743549.2:n.630T>C
XR_002956292.1:n.630T>C
NM_183050.4:c.600T>C MANE Select	NP_898871.1:p.Pro200=
NR_134945.2:n.623T>C
NM_000056.5:c.600T>C	NP_000047.1:p.Pro200=