Canonical Allele Identifier: CA346327488

Gene: CYP1B1

Linked Data

• dbSNP Id: rs2125314756
• MyVariant Identifiers: chr2:g.38298218C>T (hg19) ; chr2:g.38071075C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38071075C>T , CM000664.2:g.38071075C>T	GRCh38
NC_000002.11:g.38298218C>T , CM000664.1:g.38298218C>T	GRCh37
NC_000002.10:g.38151722C>T	NCBI36
NG_008386.2:g.10027G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000490576.2:c.1279G>A	ENSP00000478839.2:p.Val427Met
ENST00000610745.5:c.1279G>A MANE Select	ENSP00000478561.1:p.Val427Met
ENST00000492443.1:n.657G>A
ENST00000494864.1:c.166G>A	ENSP00000479876.1:p.Val56Met
ENST00000610745.4:c.1279G>A	ENSP00000478561.1:p.Val427Met
ENST00000614273.1:c.1279G>A	ENSP00000483678.1:p.Val427Met
NM_000104.3:c.1279G>A	NP_000095.2:p.Val427Met
NM_000104.4:c.1279G>A MANE Select	NP_000095.2:p.Val427Met