Canonical Allele Identifier: CA7660056

Gene: CYP1A2

Linked Data

• dbSNP Id: rs764540861
• ExAC: 15:75047117 C / T
• gnomAD v2: 15-75047117-C-T
• gnomAD v4: 15-74754776-C-T
• MyVariant Identifiers: chr15:g.75047117C>T (hg19) ; chr15:g.74754776C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754776C>T , CM000677.2:g.74754776C>T	GRCh38
NC_000015.9:g.75047117C>T , CM000677.1:g.75047117C>T	GRCh37
NC_000015.8:g.72834170C>T	NCBI36
NG_008431.1:g.37235C>T
NG_008431.2:g.37235C>T
NG_061543.1:g.10932C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1254-15C>T MANE Select	ENSP00000342007.4:n.1254-15C>T
ENST00000343932.4:c.1254-15C>T	ENSP00000342007.4:n.1254-15C>T
NM_000761.4:c.1254-15C>T	NP_000752.2:n.1254-15C>T
NM_000761.5:c.1254-15C>T MANE Select	NP_000752.2:n.1254-15C>T