Canonical Allele Identifier: CA176153952
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs924712711
gnomAD v3: 8-47960269-C-T
gnomAD v4: 8-47960269-C-T
MyVariant Identifiers: chr8:g.48872829C>T (hg19) chr8:g.47960269C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960269C>T , CM000670.2:g.47960269C>T GRCh38
NC_000008.10:g.48872829C>T , CM000670.1:g.48872829C>T GRCh37
NC_000008.9:g.49035382C>T NCBI36
NG_023435.1:g.4915G>A , LRG_162:g.4915G>A
NG_032967.1:g.5067C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-66C>T ENSP00000430329.1:n.-66C>T
NM_005914.3:c.-876C>T NP_005905.2:n.-876C>T
NM_182746.2:c.-760C>T NP_877423.1:n.-760C>T
XM_005251234.1:c.-1122C>T XP_005251291.1:n.-1122C>T
Search 100 bp 5'
Search 100 bp 3'