Canonical Allele Identifier: CA346330095

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075387A>C , CM000664.2:g.38075387A>C	GRCh38
NC_000002.11:g.38302530A>C , CM000664.1:g.38302530A>C	GRCh37
NC_000002.10:g.38156034A>C	NCBI36
NG_008386.2:g.5715T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.2T>G	ENSP00000478839.2:p.Met1Arg
ENST00000610745.5:c.2T>G MANE Select	ENSP00000478561.1:p.Met1Arg
ENST00000490576.1:c.2T>G	ENSP00000478839.1:p.Met1Arg
ENST00000494864.1:c.-70-4077T>G	ENSP00000479876.1:n.-70-4077T>G
ENST00000610745.4:c.2T>G	ENSP00000478561.1:p.Met1Arg
ENST00000613082.1:n.375+393T>G
ENST00000614273.1:c.2T>G	ENSP00000483678.1:p.Met1Arg
NM_000104.3:c.2T>G	NP_000095.2:p.Met1Arg
XM_011533236.1:c.1A>C	XP_011531538.1:p.Met1Leu
NM_000104.4:c.2T>G MANE Select	NP_000095.2:p.Met1Arg