Canonical Allele Identifier: CA2679046379
Gene: MMUT HGNC NCBI

Linked Data

gnomAD v4: 6-49447645-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447645A>C , CM000668.2:g.49447645A>C GRCh38
NC_000006.11:g.49415358A>C , CM000668.1:g.49415358A>C GRCh37
NC_000006.10:g.49523317A>C NCBI36
NG_007100.1:g.20495T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1560+25T>G MANE Select ENSP00000274813.3:n.1560+25T>G
ENST00000274813.3:c.1560+25T>G ENSP00000274813.3:n.1560+25T>G
NM_000255.3:c.1560+25T>G NP_000246.2:n.1560+25T>G
XM_005249143.2:c.1560+25T>G XP_005249200.1:n.1560+25T>G
XM_005249143.3:c.1560+25T>G XP_005249200.1:n.1560+25T>G
NM_000255.4:c.1560+25T>G MANE Select NP_000246.2:n.1560+25T>G
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