Canonical Allele Identifier: CA1245628771
Gene: CYP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1682537225
gnomAD v4: 2-38076198-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076198G>T , CM000664.2:g.38076198G>T GRCh38
NC_000002.11:g.38303340G>T , CM000664.1:g.38303340G>T GRCh37
NC_000002.10:g.38156844G>T NCBI36
NG_008386.2:g.4904C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000494864.1:c.-70-4888C>A ENSP00000479876.1:n.-70-4888C>A
XM_011533236.1:c.812G>T XP_011531538.1:p.Gly271Val