Canonical Allele Identifier: CA346327977
Gene: CYP1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.38298454C>T (hg19) chr2:g.38071311C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071311C>T , CM000664.2:g.38071311C>T GRCh38
NC_000002.11:g.38298454C>T , CM000664.1:g.38298454C>T GRCh37
NC_000002.10:g.38151958C>T NCBI36
NG_008386.2:g.9791G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1044-1G>A ENSP00000478839.2:n.1044-1G>A
ENST00000610745.5:c.1044-1G>A MANE Select ENSP00000478561.1:n.1044-1G>A
ENST00000492443.1:n.422-1G>A
ENST00000494864.1:c.-70-1G>A ENSP00000479876.1:n.-70-1G>A
ENST00000610745.4:c.1044-1G>A ENSP00000478561.1:n.1044-1G>A
ENST00000613082.1:n.439-1G>A
ENST00000614273.1:c.1044-1G>A ENSP00000483678.1:n.1044-1G>A
NM_000104.3:c.1044-1G>A NP_000095.2:n.1044-1G>A
NM_000104.4:c.1044-1G>A MANE Select NP_000095.2:n.1044-1G>A
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