Canonical Allele Identifier: CA7659794

Gene: CYP1A2

Linked Data

• dbSNP Id: rs775943025
• ExAC: 15:75042544 CTCA / C
• gnomAD v2: 15-75042544-CTCA-C
• gnomAD v3: 15-74750203-CTCA-C
• gnomAD v4: 15-74750203-CTCA-C
• MyVariant Identifiers: chr15:g.75042545_75042547del (hg19) ; chr15:g.74750205_74750207del (hg38) ; chr15:g.74750204_74750206del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74750206_74750208del , CM000677.2:g.74750206_74750208del	GRCh38
NC_000015.9:g.75042547_75042549del , CM000677.1:g.75042547_75042549del	GRCh37
NC_000015.8:g.72829600_72829602del	NCBI36
NG_008431.1:g.32665_32667del
NG_008431.2:g.32665_32667del
NG_061543.1:g.6362_6364del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.468_470del MANE Select	ENSP00000342007.4:p.Ser157del
ENST00000343932.4:c.468_470del	ENSP00000342007.4:p.Ser157del
NM_000761.4:c.468_470del	NP_000752.2:p.Ser157del
NM_000761.5:c.468_470del MANE Select	NP_000752.2:p.Ser157del