Canonical Allele Identifier: CA405965621
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40848638-T-C
MyVariant Identifiers: chr19:g.41354543T>C (hg19) chr19:g.40848638T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848638T>C , CM000681.2:g.40848638T>C GRCh38
NC_000019.9:g.41354543T>C , CM000681.1:g.41354543T>C GRCh37
NC_000019.8:g.46046383T>C NCBI36
NG_008377.1:g.6810A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.469A>G MANE Select ENSP00000301141.4:p.Ile157Val
ENST00000301141.9:c.469A>G ENSP00000301141.4:p.Ile157Val
ENST00000596719.5:n.320A>G
ENST00000600495.1:c.*281A>G ENSP00000472905.1:n.*281A>G
ENST00000601627.1:c.120-43353T>C
ENST00000610301.1:c.469A>G ENSP00000477899.1:p.Ile157Val
NM_000762.5:c.469A>G NP_000753.3:p.Ile157Val
NM_000762.6:c.469A>G MANE Select NP_000753.3:p.Ile157Val
Search 100 bp 5'
Search 100 bp 3'