Canonical Allele Identifier: CA346330021
Gene: CYP1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.38302494A>C (hg19) chr2:g.38075351A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075351A>C , CM000664.2:g.38075351A>C GRCh38
NC_000002.11:g.38302494A>C , CM000664.1:g.38302494A>C GRCh37
NC_000002.10:g.38155998A>C NCBI36
NG_008386.2:g.5751T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.38T>G ENSP00000478839.2:p.Leu13Arg
ENST00000610745.5:c.38T>G MANE Select ENSP00000478561.1:p.Leu13Arg
ENST00000490576.1:c.38T>G ENSP00000478839.1:p.Leu13Arg
ENST00000494864.1:c.-70-4041T>G ENSP00000479876.1:n.-70-4041T>G
ENST00000610745.4:c.38T>G ENSP00000478561.1:p.Leu13Arg
ENST00000613082.1:n.375+429T>G
ENST00000614273.1:c.38T>G ENSP00000483678.1:p.Leu13Arg
NM_000104.3:c.38T>G NP_000095.2:p.Leu13Arg
NM_000104.4:c.38T>G MANE Select NP_000095.2:p.Leu13Arg
Search 100 bp 5'
Search 100 bp 3'