Canonical Allele Identifier: CA358946997
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115748T>G (hg19) chr4:g.186194594T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194594T>G , CM000666.2:g.186194594T>G GRCh38
NC_000004.11:g.187115748T>G , CM000666.1:g.187115748T>G GRCh37
NC_000004.10:g.187352742T>G NCBI36
NG_007965.1:g.8075T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.309T>G MANE Select ENSP00000368079.4:p.Tyr103Ter
ENST00000378802.4:c.309T>G ENSP00000368079.4:p.Tyr103Ter
NM_207352.3:c.309T>G NP_997235.3:p.Tyr103Ter
XM_005262935.2:c.309T>G XP_005262992.1:p.Tyr103Ter
XM_006714184.2:c.-2T>G XP_006714247.1:n.-2T>G
XM_005262935.4:c.309T>G XP_005262992.1:p.Tyr103Ter
XM_017008037.1:c.-2T>G XP_016863526.1:n.-2T>G
NM_207352.4:c.309T>G MANE Select NP_997235.3:p.Tyr103Ter
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