Canonical Allele Identifier: CA358947727
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1283933679

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197549G>T , CM000666.2:g.186197549G>T GRCh38
NC_000004.11:g.187118703G>T , CM000666.1:g.187118703G>T GRCh37
NC_000004.10:g.187355697G>T NCBI36
NG_007965.1:g.11030G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.621G>T MANE Select ENSP00000368079.4:p.Lys207Asn
ENST00000378802.4:c.621G>T ENSP00000368079.4:p.Lys207Asn
ENST00000507209.5:n.1462G>T
NM_207352.3:c.621G>T NP_997235.3:p.Lys207Asn
XM_005262935.2:c.621G>T XP_005262992.1:p.Lys207Asn
XM_006714184.2:c.225G>T XP_006714247.1:p.Lys75Asn
XM_005262935.4:c.621G>T XP_005262992.1:p.Lys207Asn
XM_017008037.1:c.225G>T XP_016863526.1:p.Lys75Asn
NM_207352.4:c.621G>T MANE Select NP_997235.3:p.Lys207Asn