Canonical Allele Identifier: CA1781909204
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090793142
gnomAD v4: 8-47960246-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960246A>G , CM000670.2:g.47960246A>G GRCh38
NC_000008.10:g.48872806A>G , CM000670.1:g.48872806A>G GRCh37
NC_000008.9:g.49035359A>G NCBI36
NG_023435.1:g.4938T>C , LRG_162:g.4938T>C
NG_032967.1:g.5044A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-89A>G ENSP00000430329.1:n.-89A>G
NM_005914.3:c.-899A>G NP_005905.2:n.-899A>G
NM_182746.2:c.-783A>G NP_877423.1:n.-783A>G