Canonical Allele Identifier: CA364404873
Gene: MMUT HGNC NCBI

Linked Data

gnomAD v4: 6-49459091-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459091T>G , CM000668.2:g.49459091T>G GRCh38
NC_000006.11:g.49426804T>G , CM000668.1:g.49426804T>G GRCh37
NC_000006.10:g.49534763T>G NCBI36
NG_007100.1:g.9049A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.376A>C MANE Select ENSP00000274813.3:p.Asn126His
ENST00000274813.3:c.376A>C ENSP00000274813.3:p.Asn126His
NM_000255.3:c.376A>C NP_000246.2:p.Asn126His
XM_005249143.2:c.376A>C XP_005249200.1:p.Asn126His
XM_005249143.3:c.376A>C XP_005249200.1:p.Asn126His
NM_000255.4:c.376A>C MANE Select NP_000246.2:p.Asn126His