Canonical Allele Identifier: CA7659965
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs776247561

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752102G>T , CM000677.2:g.74752102G>T GRCh38
NC_000015.9:g.75044443G>T , CM000677.1:g.75044443G>T GRCh37
NC_000015.8:g.72831496G>T NCBI36
NG_008431.1:g.34561G>T
NG_008431.2:g.34561G>T
NG_061543.1:g.8258G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1043-22G>T MANE Select ENSP00000342007.4:n.1043-22G>T
ENST00000343932.4:c.1043-22G>T ENSP00000342007.4:n.1043-22G>T
NM_000761.4:c.1043-22G>T NP_000752.2:n.1043-22G>T
NM_000761.5:c.1043-22G>T MANE Select NP_000752.2:n.1043-22G>T