Canonical Allele Identifier: CA2749545434
Gene: CYP1B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075502A>T , CM000664.2:g.38075502A>T GRCh38
NC_000002.11:g.38302645A>T , CM000664.1:g.38302645A>T GRCh37
NC_000002.10:g.38156149A>T NCBI36
NG_008386.2:g.5600T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-113T>A ENSP00000478839.2:n.-1-113T>A
ENST00000610745.5:c.-1-113T>A MANE Select ENSP00000478561.1:n.-1-113T>A
ENST00000490576.1:c.-1-113T>A ENSP00000478839.1:n.-1-113T>A
ENST00000494864.1:c.-70-4192T>A ENSP00000479876.1:n.-70-4192T>A
ENST00000610745.4:c.-1-113T>A ENSP00000478561.1:n.-1-113T>A
ENST00000613082.1:n.375+278T>A
ENST00000614273.1:c.-1-113T>A ENSP00000483678.1:n.-1-113T>A
NM_000104.3:c.-1-113T>A NP_000095.2:n.-1-113T>A
XM_011533236.1:c.116A>T XP_011531538.1:p.Glu39Val
NM_000104.4:c.-1-113T>A MANE Select NP_000095.2:n.-1-113T>A
Search 100 bp 5'
Search 100 bp 3'