Canonical Allele Identifier: CA2658667978
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38075584-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075584T>C , CM000664.2:g.38075584T>C GRCh38
NC_000002.11:g.38302727T>C , CM000664.1:g.38302727T>C GRCh37
NC_000002.10:g.38156231T>C NCBI36
NG_008386.2:g.5518A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-195A>G ENSP00000478839.2:n.-1-195A>G
ENST00000610745.5:c.-1-195A>G MANE Select ENSP00000478561.1:n.-1-195A>G
ENST00000490576.1:c.-1-195A>G ENSP00000478839.1:n.-1-195A>G
ENST00000494864.1:c.-70-4274A>G ENSP00000479876.1:n.-70-4274A>G
ENST00000610745.4:c.-1-195A>G ENSP00000478561.1:n.-1-195A>G
ENST00000613082.1:n.375+196A>G
ENST00000614273.1:c.-2+192A>G ENSP00000483678.1:n.-2+192A>G
NM_000104.3:c.-1-195A>G NP_000095.2:n.-1-195A>G
XM_011533236.1:c.198T>C XP_011531538.1:p.Phe66=
NM_000104.4:c.-1-195A>G MANE Select NP_000095.2:n.-1-195A>G
Search 100 bp 5'
Search 100 bp 3'