Canonical Allele Identifier: CA14148631

Gene: CYP1A2

Linked Data

• dbSNP Id: rs3743484
• gnomAD v2: 15-75044400-G-C
• gnomAD v3: 15-74752059-G-C
• gnomAD v4: 15-74752059-G-C
• MyVariant Identifiers: chr15:g.75044400G>C (hg19) ; chr15:g.74752059G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74752059G>C , CM000677.2:g.74752059G>C	GRCh38
NC_000015.9:g.75044400G>C , CM000677.1:g.75044400G>C	GRCh37
NC_000015.8:g.72831453G>C	NCBI36
NG_008431.1:g.34518G>C
NG_008431.2:g.34518G>C
NG_061543.1:g.8215G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1043-65G>C MANE Select	ENSP00000342007.4:n.1043-65G>C
ENST00000343932.4:c.1043-65G>C	ENSP00000342007.4:n.1043-65G>C
NM_000761.4:c.1043-65G>C	NP_000752.2:n.1043-65G>C
NM_000761.5:c.1043-65G>C MANE Select	NP_000752.2:n.1043-65G>C