Canonical Allele Identifier: CA138800798
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1045562517
gnomAD v4: 6-49458984-G-C
MyVariant Identifiers: chr6:g.49426697G>C (hg19) chr6:g.49458984G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458984G>C , CM000668.2:g.49458984G>C GRCh38
NC_000006.11:g.49426697G>C , CM000668.1:g.49426697G>C GRCh37
NC_000006.10:g.49534656G>C NCBI36
NG_007100.1:g.9156C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.385+98C>G MANE Select ENSP00000274813.3:n.385+98C>G
ENST00000274813.3:c.385+98C>G ENSP00000274813.3:n.385+98C>G
NM_000255.3:c.385+98C>G NP_000246.2:n.385+98C>G
XM_005249143.2:c.385+98C>G XP_005249200.1:n.385+98C>G
XM_005249143.3:c.385+98C>G XP_005249200.1:n.385+98C>G
NM_000255.4:c.385+98C>G MANE Select NP_000246.2:n.385+98C>G
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