Canonical Allele Identifier: CA346327666
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071162T>C , CM000664.2:g.38071162T>C GRCh38
NC_000002.11:g.38298305T>C , CM000664.1:g.38298305T>C GRCh37
NC_000002.10:g.38151809T>C NCBI36
NG_008386.2:g.9940A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.1192A>G ENSP00000478839.2:p.Thr398Ala
ENST00000610745.5:c.1192A>G MANE Select ENSP00000478561.1:p.Thr398Ala
ENST00000492443.1:n.570A>G
ENST00000494864.1:c.79A>G ENSP00000479876.1:p.Thr27Ala
ENST00000610745.4:c.1192A>G ENSP00000478561.1:p.Thr398Ala
ENST00000614273.1:c.1192A>G ENSP00000483678.1:p.Thr398Ala
NM_000104.3:c.1192A>G NP_000095.2:p.Thr398Ala
NM_000104.4:c.1192A>G MANE Select NP_000095.2:p.Thr398Ala