Canonical Allele Identifier: CA425864674
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38075032-G-T
MyVariant Identifiers: chr2:g.38302175G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075032G>T , CM000664.2:g.38075032G>T GRCh38
NC_000002.11:g.38302175G>T , CM000664.1:g.38302175G>T GRCh37
NC_000002.10:g.38155679G>T NCBI36
NG_008386.2:g.6070C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.357C>A ENSP00000478839.2:p.Ala119=
ENST00000610745.5:c.357C>A MANE Select ENSP00000478561.1:p.Ala119=
ENST00000490576.1:c.357C>A ENSP00000478839.1:p.Ala119=
ENST00000494864.1:c.-70-3722C>A ENSP00000479876.1:n.-70-3722C>A
ENST00000610745.4:c.357C>A ENSP00000478561.1:p.Ala119=
ENST00000613082.1:n.376-624C>A
ENST00000614273.1:c.357C>A ENSP00000483678.1:p.Ala119=
NM_000104.3:c.357C>A NP_000095.2:p.Ala119=
NM_000104.4:c.357C>A MANE Select NP_000095.2:p.Ala119=
Search 100 bp 5'
Search 100 bp 3'