Canonical Allele Identifier: CA507687990
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41351205G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845300G>C , CM000681.2:g.40845300G>C GRCh38
NC_000019.9:g.41351205G>C , CM000681.1:g.41351205G>C GRCh37
NC_000019.8:g.46043045G>C NCBI36
NG_008377.1:g.10148C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1155C>G MANE Select ENSP00000301141.4:p.Leu385=
ENST00000301141.9:c.1155C>G ENSP00000301141.4:p.Leu385=
ENST00000596719.5:n.1006C>G
ENST00000601627.1:c.119+43885G>C
ENST00000610301.1:c.1155C>G ENSP00000477899.1:p.Leu385=
NM_000762.5:c.1155C>G NP_000753.3:p.Leu385=
NM_000762.6:c.1155C>G MANE Select NP_000753.3:p.Leu385=
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Search 100 bp 3'