Canonical Allele Identifier: CA425864422
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38070863-T-C
MyVariant Identifiers: chr2:g.38298006T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38070863T>C , CM000664.2:g.38070863T>C GRCh38
NC_000002.11:g.38298006T>C , CM000664.1:g.38298006T>C GRCh37
NC_000002.10:g.38151510T>C NCBI36
NG_008386.2:g.10239A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1491A>G ENSP00000478839.2:p.Pro497=
ENST00000610745.5:c.1491A>G MANE Select ENSP00000478561.1:p.Pro497=
ENST00000494864.1:c.378A>G ENSP00000479876.1:p.Pro126=
ENST00000610745.4:c.1491A>G ENSP00000478561.1:p.Pro497=
ENST00000614273.1:c.1491A>G ENSP00000483678.1:p.Pro497=
NM_000104.3:c.1491A>G NP_000095.2:p.Pro497=
NM_000104.4:c.1491A>G MANE Select NP_000095.2:p.Pro497=
Search 100 bp 5'
Search 100 bp 3'