Canonical Allele Identifier: CA2749544721

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38071312_38071313insACA , CM000664.2:g.38071312_38071313insACA	GRCh38
NC_000002.11:g.38298455_38298456insACA , CM000664.1:g.38298455_38298456insACA	GRCh37
NC_000002.10:g.38151959_38151960insACA	NCBI36
NG_008386.2:g.9789_9790insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.1044-3_1044-2insTGT	ENSP00000478839.2:n.1044-3_1044-2insTGT
ENST00000610745.5:c.1044-3_1044-2insTGT MANE Select	ENSP00000478561.1:n.1044-3_1044-2insTGT
ENST00000492443.1:n.422-3_422-2insTGT
ENST00000494864.1:c.-70-3_-70-2insTGT	ENSP00000479876.1:n.-70-3_-70-2insTGT
ENST00000610745.4:c.1044-3_1044-2insTGT	ENSP00000478561.1:n.1044-3_1044-2insTGT
ENST00000613082.1:n.439-3_439-2insTGT
ENST00000614273.1:c.1044-3_1044-2insTGT	ENSP00000483678.1:n.1044-3_1044-2insTGT
NM_000104.3:c.1044-3_1044-2insTGT	NP_000095.2:n.1044-3_1044-2insTGT
NM_000104.4:c.1044-3_1044-2insTGT MANE Select	NP_000095.2:n.1044-3_1044-2insTGT