Canonical Allele Identifier: CA308499375

Gene: CYP2B6

Linked Data

• dbSNP Id: rs924036592
• gnomAD v3: 19-41012926-T-G
• gnomAD v4: 19-41012926-T-G
• MyVariant Identifiers: chr19:g.41518831T>G (hg19) ; chr19:g.41012926T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012926T>G , CM000681.2:g.41012926T>G	GRCh38
NC_000019.9:g.41518831T>G , CM000681.1:g.41518831T>G	GRCh37
NC_000019.8:g.46210671T>G	NCBI36
NG_007929.1:g.26628T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1294+111T>G MANE Select	ENSP00000324648.2:n.1294+111T>G
ENST00000598834.2:c.1177-47T>G
ENST00000324071.8:c.1294+111T>G	ENSP00000324648.2:n.1294+111T>G
ENST00000593831.1:c.586+111T>G	ENSP00000470582.1:n.586+111T>G
ENST00000597612.1:n.647+441T>G
NM_000767.4:c.1294+111T>G	NP_000758.1:n.1294+111T>G
XM_005258569.3:c.1152+441T>G	XP_005258626.1:n.1152+441T>G
XM_006723050.2:c.1295-47T>G	XP_006723113.1:n.1295-47T>G
XM_011526546.1:c.*12T>G	XP_011524848.1:n.*12T>G
XM_011526547.1:c.1153-47T>G	XP_011524849.1:n.1153-47T>G
XM_011526548.1:c.814+111T>G	XP_011524850.1:n.814+111T>G
XM_011526549.1:c.703+111T>G	XP_011524851.1:n.703+111T>G
XM_011526550.1:c.694+111T>G	XP_011524852.1:n.694+111T>G
NM_000767.5:c.1294+111T>G MANE Select	NP_000758.1:n.1294+111T>G