Canonical Allele Identifier: CA442882087
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187130107T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208953T>G , CM000666.2:g.186208953T>G GRCh38
NC_000004.11:g.187130107T>G , CM000666.1:g.187130107T>G GRCh37
NC_000004.10:g.187367101T>G NCBI36
NG_007965.1:g.22434T>G
NG_012095.2:g.4975T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1179T>G MANE Select ENSP00000368079.4:p.Pro393=
ENST00000378802.4:c.1179T>G ENSP00000368079.4:p.Pro393=
ENST00000502665.1:n.414T>G
ENST00000507209.5:n.5877T>G
ENST00000513354.5:n.269T>G
NM_207352.3:c.1179T>G NP_997235.3:p.Pro393=
XM_005262935.2:c.1179T>G XP_005262992.1:p.Pro393=
XM_006714184.2:c.783T>G XP_006714247.1:p.Pro261=
XM_005262935.4:c.1179T>G XP_005262992.1:p.Pro393=
XM_017008037.1:c.783T>G XP_016863526.1:p.Pro261=
NM_207352.4:c.1179T>G MANE Select NP_997235.3:p.Pro393=