Canonical Allele Identifier: CA7659962

Gene: CYP1A2

Linked Data

• dbSNP Id: rs373310437
• ExAC: 15:75044425 G / C
• gnomAD v2: 15-75044425-G-C
• gnomAD v3: 15-74752084-G-C
• gnomAD v4: 15-74752084-G-C
• MyVariant Identifiers: chr15:g.75044425G>C (hg19) ; chr15:g.74752084G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74752084G>C , CM000677.2:g.74752084G>C	GRCh38
NC_000015.9:g.75044425G>C , CM000677.1:g.75044425G>C	GRCh37
NC_000015.8:g.72831478G>C	NCBI36
NG_008431.1:g.34543G>C
NG_008431.2:g.34543G>C
NG_061543.1:g.8240G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1043-40G>C MANE Select	ENSP00000342007.4:n.1043-40G>C
ENST00000343932.4:c.1043-40G>C	ENSP00000342007.4:n.1043-40G>C
NM_000761.4:c.1043-40G>C	NP_000752.2:n.1043-40G>C
NM_000761.5:c.1043-40G>C MANE Select	NP_000752.2:n.1043-40G>C