Canonical Allele Identifier: CA1519919025
Gene: CYP4V2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197327C= , CM000666.2:g.186197327C= GRCh38
NC_000004.11:g.187118481C= , CM000666.1:g.187118481C= GRCh37
NC_000004.10:g.187355475C= NCBI36
NG_007965.1:g.10808C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.604+197C= MANE Select ENSP00000368079.4:n.604+197C=
ENST00000378802.4:c.604+197C= ENSP00000368079.4:n.604+197C=
ENST00000507209.5:n.1240C=
NM_207352.3:c.604+197C= NP_997235.3:n.604+197C=
XM_005262935.2:c.604+197C= XP_005262992.1:n.604+197C=
XM_006714184.2:c.208+197C= XP_006714247.1:n.208+197C=
XM_005262935.4:c.604+197C= XP_005262992.1:n.604+197C=
XM_017008037.1:c.208+197C= XP_016863526.1:n.208+197C=
NM_207352.4:c.604+197C= MANE Select NP_997235.3:n.604+197C=
Search 100 bp 5'
Search 100 bp 3'