Canonical Allele Identifier: CA768426527

Gene: CYP1B1

Linked Data

• dbSNP Id: rs1392416502
• gnomAD v3: 2-38075624-C-G
• gnomAD v4: 2-38075624-C-G
• MyVariant Identifiers: chr2:g.38302767C>G (hg19) ; chr2:g.38075624C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075624C>G , CM000664.2:g.38075624C>G	GRCh38
NC_000002.11:g.38302767C>G , CM000664.1:g.38302767C>G	GRCh37
NC_000002.10:g.38156271C>G	NCBI36
NG_008386.2:g.5478G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-235G>C	ENSP00000478839.2:n.-1-235G>C
ENST00000610745.5:c.-2+156G>C MANE Select	ENSP00000478561.1:n.-2+156G>C
ENST00000490576.1:c.-1-235G>C	ENSP00000478839.1:n.-1-235G>C
ENST00000494864.1:c.-70-4314G>C	ENSP00000479876.1:n.-70-4314G>C
ENST00000610745.4:c.-2+156G>C	ENSP00000478561.1:n.-2+156G>C
ENST00000613082.1:n.375+156G>C
ENST00000614273.1:c.-2+152G>C	ENSP00000483678.1:n.-2+152G>C
NM_000104.3:c.-2+156G>C	NP_000095.2:n.-2+156G>C
XM_011533236.1:c.238C>G	XP_011531538.1:p.Arg80Gly
NM_000104.4:c.-2+156G>C MANE Select	NP_000095.2:n.-2+156G>C