Canonical Allele Identifier: CA364404070
Gene: MMUT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.49425466A>C (hg19) chr6:g.49457753A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49457753A>C , CM000668.2:g.49457753A>C GRCh38
NC_000006.11:g.49425466A>C , CM000668.1:g.49425466A>C GRCh37
NC_000006.10:g.49533425A>C NCBI36
NG_007100.1:g.10387T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.691T>G MANE Select ENSP00000274813.3:p.Tyr231Asp
ENST00000274813.3:c.691T>G ENSP00000274813.3:p.Tyr231Asp
NM_000255.3:c.691T>G NP_000246.2:p.Tyr231Asp
XM_005249143.2:c.691T>G XP_005249200.1:p.Tyr231Asp
XM_005249143.3:c.691T>G XP_005249200.1:p.Tyr231Asp
NM_000255.4:c.691T>G MANE Select NP_000246.2:p.Tyr231Asp
Search 100 bp 5'
Search 100 bp 3'