Canonical Allele Identifier: CA12385925

Linked Data

dbSNP Id: rs3132581
gnomAD v2: 6-30913458-G-A
gnomAD v3: 6-30945681-G-A
gnomAD v4: 6-30945681-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30945681G>A , CM000668.2:g.30945681G>A GRCh38
NC_000006.11:g.30913458G>A , CM000668.1:g.30913458G>A GRCh37
NC_000006.10:g.31021437G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000462446.6:c.83-2866G>A (MUCL3) MANE Select ENSP00000417182.1:n.83-2866G>A
ENST00000636043.1:c.284-2866G>A (MUCL3) ENSP00000490368.1:n.284-2866G>A
ENST00000304311.3:c.83-2866G>A (MUCL3) ENSP00000305948.3:n.83-2866G>A
ENST00000462446.5:c.83-2866G>A (MUCL3) ENSP00000417182.1:n.83-2866G>A
ENST00000634371.1:c.-9+6681C>T (SFTA2) ENSP00000489572.1:n.-9+6681C>T
NM_080870.3:c.83-2866G>A (MUCL3) NP_543146.2:n.83-2866G>A
NM_080870.4:c.83-2866G>A (MUCL3) MANE Select NP_543146.2:n.83-2866G>A