Canonical Allele Identifier: CA425864494
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38071058-C-T
MyVariant Identifiers: chr2:g.38298201C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071058C>T , CM000664.2:g.38071058C>T GRCh38
NC_000002.11:g.38298201C>T , CM000664.1:g.38298201C>T GRCh37
NC_000002.10:g.38151705C>T NCBI36
NG_008386.2:g.10044G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1296G>A ENSP00000478839.2:p.Leu432=
ENST00000610745.5:c.1296G>A MANE Select ENSP00000478561.1:p.Leu432=
ENST00000492443.1:n.674G>A
ENST00000494864.1:c.183G>A ENSP00000479876.1:p.Leu61=
ENST00000610745.4:c.1296G>A ENSP00000478561.1:p.Leu432=
ENST00000614273.1:c.1296G>A ENSP00000483678.1:p.Leu432=
NM_000104.3:c.1296G>A NP_000095.2:p.Leu432=
NM_000104.4:c.1296G>A MANE Select NP_000095.2:p.Leu432=
Search 100 bp 5'
Search 100 bp 3'