Canonical Allele Identifier: CA2658668062
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38075628-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075628A>G , CM000664.2:g.38075628A>G GRCh38
NC_000002.11:g.38302771A>G , CM000664.1:g.38302771A>G GRCh37
NC_000002.10:g.38156275A>G NCBI36
NG_008386.2:g.5474T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-239T>C ENSP00000478839.2:n.-1-239T>C
ENST00000610745.5:c.-2+152T>C MANE Select ENSP00000478561.1:n.-2+152T>C
ENST00000490576.1:c.-1-239T>C ENSP00000478839.1:n.-1-239T>C
ENST00000494864.1:c.-70-4318T>C ENSP00000479876.1:n.-70-4318T>C
ENST00000610745.4:c.-2+152T>C ENSP00000478561.1:n.-2+152T>C
ENST00000613082.1:n.375+152T>C
ENST00000614273.1:c.-2+148T>C ENSP00000483678.1:n.-2+148T>C
NM_000104.3:c.-2+152T>C NP_000095.2:n.-2+152T>C
XM_011533236.1:c.242A>G XP_011531538.1:p.Lys81Arg
NM_000104.4:c.-2+152T>C MANE Select NP_000095.2:n.-2+152T>C
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