Canonical Allele Identifier: CA633140826

Gene: CYP2A6

Linked Data

• dbSNP Id: rs1393645351
• gnomAD v2: 19-41353946-AGGGTATTGGACATCCATCCT-A
• gnomAD v3: 19-40848041-AGGGTATTGGACATCCATCCT-A
• gnomAD v4: 19-40848041-AGGGTATTGGACATCCATCCT-A
• MyVariant Identifiers: chr19:g.41353947_41353966del (hg19) ; chr19:g.40848042_40848061del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848046_40848065del , CM000681.2:g.40848046_40848065del	GRCh38
NC_000019.9:g.41353951_41353970del , CM000681.1:g.41353951_41353970del	GRCh37
NC_000019.8:g.46045791_46045810del	NCBI36
NG_008377.1:g.7387_7406del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.654+158_654+177del MANE Select	ENSP00000301141.4:n.654+158_654+177del
ENST00000301141.9:c.654+158_654+177del	ENSP00000301141.4:n.654+158_654+177del
ENST00000596719.5:n.505+158_505+177del
ENST00000600495.1:c.*466+158_*466+177del	ENSP00000472905.1:n.*466+158_*466+177del
ENST00000601627.1:c.120-43945_120-43926del
ENST00000610301.1:c.654+158_654+177del	ENSP00000477899.1:n.654+158_654+177del
NM_000762.5:c.654+158_654+177del	NP_000753.3:n.654+158_654+177del
NM_000762.6:c.654+158_654+177del MANE Select	NP_000753.3:n.654+158_654+177del