Canonical Allele Identifier: CA757434439

Gene: MCM6

Linked Data

• dbSNP Id: rs1354465426
• MyVariant Identifiers: chr2:g.136608762_136608765del (hg19) ; chr2:g.135851192_135851195del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135851193_135851196del , CM000664.2:g.135851193_135851196del	GRCh38
NC_000002.11:g.136608763_136608766del , CM000664.1:g.136608763_136608766del	GRCh37
NC_000002.10:g.136325233_136325236del	NCBI36
NG_008104.2:g.8975_8978del , LRG_338:g.8975_8978del
NG_008958.1:g.30247_30250del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264156.3:c.1917+207_1917+210del MANE Select	ENSP00000264156.2:n.1917+207_1917+210del
ENST00000264156.2:c.1917+207_1917+210del	ENSP00000264156.2:n.1917+207_1917+210del
ENST00000483902.1:n.544+207_544+210del
ENST00000492091.1:n.343+207_343+210del
NM_005915.5:c.1917+207_1917+210del	NP_005906.2:n.1917+207_1917+210del
NM_005915.6:c.1917+207_1917+210del MANE Select	NP_005906.2:n.1917+207_1917+210del