Canonical Allele Identifier: CA2679047231
Gene: MMUT HGNC NCBI

Linked Data

gnomAD v4: 6-49458986-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458986G>A , CM000668.2:g.49458986G>A GRCh38
NC_000006.11:g.49426699G>A , CM000668.1:g.49426699G>A GRCh37
NC_000006.10:g.49534658G>A NCBI36
NG_007100.1:g.9154C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.385+96C>T MANE Select ENSP00000274813.3:n.385+96C>T
ENST00000274813.3:c.385+96C>T ENSP00000274813.3:n.385+96C>T
NM_000255.3:c.385+96C>T NP_000246.2:n.385+96C>T
XM_005249143.2:c.385+96C>T XP_005249200.1:n.385+96C>T
XM_005249143.3:c.385+96C>T XP_005249200.1:n.385+96C>T
NM_000255.4:c.385+96C>T MANE Select NP_000246.2:n.385+96C>T
Search 100 bp 5'
Search 100 bp 3'