Canonical Allele Identifier: CA7659952

Gene: CYP1A2

Linked Data

• dbSNP Id: rs774462777
• ExAC: 15:75044213 ACCCTATAG / A
• gnomAD v2: 15-75044213-ACCCTATAG-A
• gnomAD v3: 15-74751872-ACCCTATAG-A
• gnomAD v4: 15-74751872-ACCCTATAG-A
• MyVariant Identifiers: chr15:g.75044214_75044221del (hg19) ; chr15:g.74751873_74751880del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74751875_74751882del , CM000677.2:g.74751875_74751882del	GRCh38
NC_000015.9:g.75044216_75044223del , CM000677.1:g.75044216_75044223del	GRCh37
NC_000015.8:g.72831269_72831276del	NCBI36
NG_008431.1:g.34334_34341del
NG_008431.2:g.34334_34341del
NG_061543.1:g.8031_8038del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1042+21_1042+28del MANE Select	ENSP00000342007.4:n.1042+21_1042+28del
ENST00000343932.4:c.1042+21_1042+28del	ENSP00000342007.4:n.1042+21_1042+28del
NM_000761.4:c.1042+21_1042+28del	NP_000752.2:n.1042+21_1042+28del
NM_000761.5:c.1042+21_1042+28del MANE Select	NP_000752.2:n.1042+21_1042+28del