Canonical Allele Identifier: CA15377719
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs4078252
gnomAD v2: 5-112455467-C-T
gnomAD v3: 5-113119770-C-T
gnomAD v4: 5-113119770-C-T
MyVariant Identifiers: chr5:g.112455467C>T (hg19) chr5:g.113119770C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113119770C>T , CM000667.2:g.113119770C>T GRCh38
NC_000005.9:g.112455467C>T , CM000667.1:g.112455467C>T GRCh37
NC_000005.8:g.112483366C>T NCBI36
NG_012265.1:g.374061G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000302475.9:c.457+2914G>A ENSP00000305617.4:n.457+2914G>A
ENST00000408903.7:c.1027+2914G>A MANE Select ENSP00000386227.3:n.1027+2914G>A
ENST00000302475.8:c.457+2914G>A ENSP00000305617.4:n.457+2914G>A
ENST00000408903.6:c.1027+2914G>A ENSP00000386227.3:n.1027+2914G>A
ENST00000502648.5:n.147+2914G>A
ENST00000506605.6:n.481+2914G>A
ENST00000511847.2:n.464+2914G>A
ENST00000514701.5:c.457+2914G>A ENSP00000485220.1:n.457+2914G>A
ENST00000515367.6:c.268+2914G>A ENSP00000421615.2:n.268+2914G>A
NM_001085377.1:c.1027+2914G>A NP_001078846.1:n.1027+2914G>A
NM_002387.2:c.457+2914G>A NP_002378.1:n.457+2914G>A
XM_005271991.2:c.457+2914G>A XP_005272048.1:n.457+2914G>A
XM_005271991.3:c.457+2914G>A XP_005272048.1:n.457+2914G>A
XM_017009473.1:c.1027+2914G>A XP_016864962.1:n.1027+2914G>A
XM_017009474.1:c.427+2914G>A XP_016864963.1:n.427+2914G>A
XM_024446049.1:c.268+2914G>A XP_024301817.1:n.268+2914G>A
XM_024446050.1:c.268+2914G>A XP_024301818.1:n.268+2914G>A
XM_024446051.1:c.268+2914G>A XP_024301819.1:n.268+2914G>A
XM_024446052.1:c.268+2914G>A XP_024301820.1:n.268+2914G>A
NM_001085377.2:c.1027+2914G>A MANE Select NP_001078846.2:n.1027+2914G>A
NM_002387.3:c.457+2914G>A NP_002378.2:n.457+2914G>A
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