Canonical Allele Identifier: CA792315763
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1351956177
gnomAD v4: 4-186191811-G-T
MyVariant Identifiers: chr4:g.187112965G>T (hg19) chr4:g.186191811G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191811G>T , CM000666.2:g.186191811G>T GRCh38
NC_000004.11:g.187112965G>T , CM000666.1:g.187112965G>T GRCh37
NC_000004.10:g.187349959G>T NCBI36
NG_007965.1:g.5292G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-13G>T MANE Select ENSP00000368079.4:n.-13G>T
ENST00000378802.4:c.-13G>T ENSP00000368079.4:n.-13G>T
NM_207352.3:c.-13G>T NP_997235.3:n.-13G>T
XM_005262935.2:c.-13G>T XP_005262992.1:n.-13G>T
XM_005262935.4:c.-13G>T XP_005262992.1:n.-13G>T
XM_017008037.1:c.-323G>T XP_016863526.1:n.-323G>T
NM_207352.4:c.-13G>T MANE Select NP_997235.3:n.-13G>T
Search 100 bp 5'
Search 100 bp 3'