Canonical Allele Identifier: CA425864773

Gene: CYP1B1

Linked Data

• dbSNP Id: rs1486123014
• gnomAD v2: 2-38302244-C-T
• gnomAD v4: 2-38075101-C-T
• MyVariant Identifiers: chr2:g.38302244C>T (hg19) ; chr2:g.38075101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075101C>T , CM000664.2:g.38075101C>T	GRCh38
NC_000002.11:g.38302244C>T , CM000664.1:g.38302244C>T	GRCh37
NC_000002.10:g.38155748C>T	NCBI36
NG_008386.2:g.6001G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.288G>A	ENSP00000478839.2:p.Val96=
ENST00000610745.5:c.288G>A MANE Select	ENSP00000478561.1:p.Val96=
ENST00000490576.1:c.288G>A	ENSP00000478839.1:p.Val96=
ENST00000494864.1:c.-70-3791G>A	ENSP00000479876.1:n.-70-3791G>A
ENST00000610745.4:c.288G>A	ENSP00000478561.1:p.Val96=
ENST00000613082.1:n.375+679G>A
ENST00000614273.1:c.288G>A	ENSP00000483678.1:p.Val96=
NM_000104.3:c.288G>A	NP_000095.2:p.Val96=
NM_000104.4:c.288G>A MANE Select	NP_000095.2:p.Val96=