Canonical Allele Identifier: CA2730938413

Gene: CYP1A2

Linked Data

• dbSNP Id: rs1257944166

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74752061G>C , CM000677.2:g.74752061G>C	GRCh38
NC_000015.9:g.75044402G>C , CM000677.1:g.75044402G>C	GRCh37
NC_000015.8:g.72831455G>C	NCBI36
NG_008431.1:g.34520G>C
NG_008431.2:g.34520G>C
NG_061543.1:g.8217G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1043-63G>C MANE Select	ENSP00000342007.4:n.1043-63G>C
ENST00000343932.4:c.1043-63G>C	ENSP00000342007.4:n.1043-63G>C
NM_000761.4:c.1043-63G>C	NP_000752.2:n.1043-63G>C
NM_000761.5:c.1043-63G>C MANE Select	NP_000752.2:n.1043-63G>C