Canonical Allele Identifier: CA2679046539
Gene: MMUT HGNC NCBI

Linked Data

gnomAD v4: 6-49448752-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49448752T>C , CM000668.2:g.49448752T>C GRCh38
NC_000006.11:g.49416465T>C , CM000668.1:g.49416465T>C GRCh37
NC_000006.10:g.49524424T>C NCBI36
NG_007100.1:g.19388A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1444+64A>G MANE Select ENSP00000274813.3:n.1444+64A>G
ENST00000274813.3:c.1444+64A>G ENSP00000274813.3:n.1444+64A>G
NM_000255.3:c.1444+64A>G NP_000246.2:n.1444+64A>G
XM_005249143.2:c.1444+64A>G XP_005249200.1:n.1444+64A>G
XM_005249143.3:c.1444+64A>G XP_005249200.1:n.1444+64A>G
NM_000255.4:c.1444+64A>G MANE Select NP_000246.2:n.1444+64A>G