Canonical Allele Identifier: CA7659963

Gene: CYP1A2

Linked Data

• dbSNP Id: rs200095478
• ExAC: 15:75044431 C / T
• gnomAD v2: 15-75044431-C-T
• gnomAD v3: 15-74752090-C-T
• gnomAD v4: 15-74752090-C-T
• MyVariant Identifiers: chr15:g.75044431C>T (hg19) ; chr15:g.74752090C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74752090C>T , CM000677.2:g.74752090C>T	GRCh38
NC_000015.9:g.75044431C>T , CM000677.1:g.75044431C>T	GRCh37
NC_000015.8:g.72831484C>T	NCBI36
NG_008431.1:g.34549C>T
NG_008431.2:g.34549C>T
NG_061543.1:g.8246C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1043-34C>T MANE Select	ENSP00000342007.4:n.1043-34C>T
ENST00000343932.4:c.1043-34C>T	ENSP00000342007.4:n.1043-34C>T
NM_000761.4:c.1043-34C>T	NP_000752.2:n.1043-34C>T
NM_000761.5:c.1043-34C>T MANE Select	NP_000752.2:n.1043-34C>T