Canonical Allele Identifier: CA2708143261
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs2126595207
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205063T>A , CM000666.2:g.186205063T>A GRCh38
NC_000004.11:g.187126217T>A , CM000666.1:g.187126217T>A GRCh37
NC_000004.10:g.187363211T>A NCBI36
NG_007965.1:g.18544T>A
NG_012095.2:g.1085T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-137T>A MANE Select ENSP00000368079.4:n.988-137T>A
ENST00000378802.4:c.988-137T>A ENSP00000368079.4:n.988-137T>A
ENST00000502665.1:n.222+5T>A
ENST00000507209.5:n.5549T>A
ENST00000513354.5:n.78-137T>A
NM_207352.3:c.988-137T>A NP_997235.3:n.988-137T>A
XM_005262935.2:c.988-137T>A XP_005262992.1:n.988-137T>A
XM_006714184.2:c.592-137T>A XP_006714247.1:n.592-137T>A
XM_005262935.4:c.988-137T>A XP_005262992.1:n.988-137T>A
XM_017008037.1:c.592-137T>A XP_016863526.1:n.592-137T>A
NM_207352.4:c.988-137T>A MANE Select NP_997235.3:n.988-137T>A
Search 100 bp 5'
Search 100 bp 3'