Canonical Allele Identifier: CA2749546769
Gene: CYP1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075598A>G , CM000664.2:g.38075598A>G GRCh38
NC_000002.11:g.38302741A>G , CM000664.1:g.38302741A>G GRCh37
NC_000002.10:g.38156245A>G NCBI36
NG_008386.2:g.5504T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-209T>C ENSP00000478839.2:n.-1-209T>C
ENST00000610745.5:c.-2+182T>C MANE Select ENSP00000478561.1:n.-2+182T>C
ENST00000490576.1:c.-1-209T>C ENSP00000478839.1:n.-1-209T>C
ENST00000494864.1:c.-70-4288T>C ENSP00000479876.1:n.-70-4288T>C
ENST00000610745.4:c.-2+182T>C ENSP00000478561.1:n.-2+182T>C
ENST00000613082.1:n.375+182T>C
ENST00000614273.1:c.-2+178T>C ENSP00000483678.1:n.-2+178T>C
NM_000104.3:c.-2+182T>C NP_000095.2:n.-2+182T>C
XM_011533236.1:c.212A>G XP_011531538.1:p.Asn71Ser
NM_000104.4:c.-2+182T>C MANE Select NP_000095.2:n.-2+182T>C
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