Canonical Allele Identifier: CA561926337
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs1308855456
gnomAD v2: 5-112723523-C-T
gnomAD v3: 5-113387826-C-T
gnomAD v4: 5-113387826-C-T
MyVariant Identifiers: chr5:g.112723523C>T (hg19) chr5:g.113387826C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387826C>T , CM000667.2:g.113387826C>T GRCh38
NC_000005.9:g.112723523C>T , CM000667.1:g.112723523C>T GRCh37
NC_000005.8:g.112751422C>T NCBI36
NG_012265.1:g.106005G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000408903.7:c.171-2614G>A MANE Select ENSP00000386227.3:n.171-2614G>A
ENST00000408903.6:c.171-2614G>A ENSP00000386227.3:n.171-2614G>A
NM_001085377.1:c.171-2614G>A NP_001078846.1:n.171-2614G>A
XM_017009473.1:c.171-2614G>A XP_016864962.1:n.171-2614G>A
NM_001085377.2:c.171-2614G>A MANE Select NP_001078846.2:n.171-2614G>A
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