Canonical Allele Identifier: CA1781909346
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090797934
gnomAD v4: 8-47960447-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960447G>C , CM000670.2:g.47960447G>C GRCh38
NC_000008.10:g.48873007G>C , CM000670.1:g.48873007G>C GRCh37
NC_000008.9:g.49035560G>C NCBI36
NG_023435.1:g.4737C>G , LRG_162:g.4737C>G
NG_032967.1:g.5245G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+127G>C ENSP00000430329.1:n.-15+127G>C
NM_005914.3:c.-698G>C NP_005905.2:n.-698G>C
NM_182746.2:c.-582G>C NP_877423.1:n.-582G>C
XM_005251234.1:c.-944G>C XP_005251291.1:n.-944G>C
Search 100 bp 5'
Search 100 bp 3'