Canonical Allele Identifier: CA425865036
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38075236-G-A
MyVariant Identifiers: chr2:g.38302379G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075236G>A , CM000664.2:g.38075236G>A GRCh38
NC_000002.11:g.38302379G>A , CM000664.1:g.38302379G>A GRCh37
NC_000002.10:g.38155883G>A NCBI36
NG_008386.2:g.5866C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.153C>T ENSP00000478839.2:p.Pro51=
ENST00000610745.5:c.153C>T MANE Select ENSP00000478561.1:p.Pro51=
ENST00000490576.1:c.153C>T ENSP00000478839.1:p.Pro51=
ENST00000494864.1:c.-70-3926C>T ENSP00000479876.1:n.-70-3926C>T
ENST00000610745.4:c.153C>T ENSP00000478561.1:p.Pro51=
ENST00000613082.1:n.375+544C>T
ENST00000614273.1:c.153C>T ENSP00000483678.1:p.Pro51=
NM_000104.3:c.153C>T NP_000095.2:p.Pro51=
NM_000104.4:c.153C>T MANE Select NP_000095.2:p.Pro51=