Canonical Allele Identifier: CA1781909186
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1356646257
gnomAD v4: 8-47960230-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960230G>T , CM000670.2:g.47960230G>T GRCh38
NC_000008.10:g.48872790G>T , CM000670.1:g.48872790G>T GRCh37
NC_000008.9:g.49035343G>T NCBI36
NG_023435.1:g.4954C>A , LRG_162:g.4954C>A
NG_032967.1:g.5028G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-105G>T ENSP00000430329.1:n.-105G>T
NM_005914.3:c.-915G>T NP_005905.2:n.-915G>T
NM_182746.2:c.-799G>T NP_877423.1:n.-799G>T
Search 100 bp 5'
Search 100 bp 3'