Canonical Allele Identifier: CA557395894
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1419119001
gnomAD v2: 4-187112974-G-C
gnomAD v4: 4-186191820-G-C
MyVariant Identifiers: chr4:g.187112974G>C (hg19) chr4:g.186191820G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191820G>C , CM000666.2:g.186191820G>C GRCh38
NC_000004.11:g.187112974G>C , CM000666.1:g.187112974G>C GRCh37
NC_000004.10:g.187349968G>C NCBI36
NG_007965.1:g.5301G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-4G>C MANE Select ENSP00000368079.4:n.-4G>C
ENST00000378802.4:c.-4G>C ENSP00000368079.4:n.-4G>C
NM_207352.3:c.-4G>C NP_997235.3:n.-4G>C
XM_005262935.2:c.-4G>C XP_005262992.1:n.-4G>C
XM_005262935.4:c.-4G>C XP_005262992.1:n.-4G>C
XM_017008037.1:c.-314G>C XP_016863526.1:n.-314G>C
NM_207352.4:c.-4G>C MANE Select NP_997235.3:n.-4G>C
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