Canonical Allele Identifier: CA3847128
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs542466439
gnomAD v2: 6-49426775-G-C
gnomAD v4: 6-49459062-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459062G>C , CM000668.2:g.49459062G>C GRCh38
NC_000006.11:g.49426775G>C , CM000668.1:g.49426775G>C GRCh37
NC_000006.10:g.49534734G>C NCBI36
NG_007100.1:g.9078C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.385+20C>G MANE Select ENSP00000274813.3:n.385+20C>G
ENST00000274813.3:c.385+20C>G ENSP00000274813.3:n.385+20C>G
NM_000255.3:c.385+20C>G NP_000246.2:n.385+20C>G
XM_005249143.2:c.385+20C>G XP_005249200.1:n.385+20C>G
XM_005249143.3:c.385+20C>G XP_005249200.1:n.385+20C>G
NM_000255.4:c.385+20C>G MANE Select NP_000246.2:n.385+20C>G