Canonical Allele Identifier: CA619121380

Gene: CYP1A2

Linked Data

• dbSNP Id: rs1191014273
• gnomAD v2: 15-75041979-C-T
• gnomAD v3: 15-74749638-C-T
• gnomAD v4: 15-74749638-C-T
• MyVariant Identifiers: chr15:g.75041979C>T (hg19) ; chr15:g.74749638C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749638C>T , CM000677.2:g.74749638C>T	GRCh38
NC_000015.9:g.75041979C>T , CM000677.1:g.75041979C>T	GRCh37
NC_000015.8:g.72829032C>T	NCBI36
NG_008431.1:g.32097C>T
NG_008431.2:g.32097C>T
NG_061543.1:g.5794C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.-9-92C>T MANE Select	ENSP00000342007.4:n.-9-92C>T
ENST00000343932.4:c.-9-92C>T	ENSP00000342007.4:n.-9-92C>T
NM_000761.4:c.-9-92C>T	NP_000752.2:n.-9-92C>T
NM_000761.5:c.-9-92C>T MANE Select	NP_000752.2:n.-9-92C>T