Canonical Allele Identifier: CA425864569

Gene: CYP1B1

Linked Data

• MyVariant Identifiers: chr2:g.38298282G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38071139G>A , CM000664.2:g.38071139G>A	GRCh38
NC_000002.11:g.38298282G>A , CM000664.1:g.38298282G>A	GRCh37
NC_000002.10:g.38151786G>A	NCBI36
NG_008386.2:g.9963C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.1215C>T	ENSP00000478839.2:p.Ala405=
ENST00000610745.5:c.1215C>T MANE Select	ENSP00000478561.1:p.Ala405=
ENST00000492443.1:n.593C>T
ENST00000494864.1:c.102C>T	ENSP00000479876.1:p.Ala34=
ENST00000610745.4:c.1215C>T	ENSP00000478561.1:p.Ala405=
ENST00000614273.1:c.1215C>T	ENSP00000483678.1:p.Ala405=
NM_000104.3:c.1215C>T	NP_000095.2:p.Ala405=
NM_000104.4:c.1215C>T MANE Select	NP_000095.2:p.Ala405=