Canonical Allele Identifier: CA154995280
Gene: MACC1 HGNC NCBI

Linked Data

dbSNP Id: rs898260054
gnomAD v3: 7-20164421-T-C
gnomAD v4: 7-20164421-T-C
MyVariant Identifiers: chr7:g.20204044T>C (hg19) chr7:g.20164421T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164421T>C , CM000669.2:g.20164421T>C GRCh38
NC_000007.13:g.20204044T>C , CM000669.1:g.20204044T>C GRCh37
NC_000007.12:g.20170569T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400331.10:c.-152-22A>G MANE Select ENSP00000383185.3:n.-152-22A>G
ENST00000332878.8:c.-8-2551A>G ENSP00000328410.4:n.-8-2551A>G
ENST00000400331.9:c.-152-22A>G ENSP00000383185.3:n.-152-22A>G
ENST00000471019.1:n.274-22A>G
ENST00000589011.1:c.-8-2551A>G ENSP00000466864.1:n.-8-2551A>G
NM_182762.3:c.-152-22A>G NP_877439.3:n.-152-22A>G
NM_182762.4:c.-152-22A>G MANE Select NP_877439.3:n.-152-22A>G
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