Canonical Allele Identifier: CA12404346
Gene: ARMC2 HGNC NCBI

Linked Data

dbSNP Id: rs2798641

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108946847C>T , CM000668.2:g.108946847C>T GRCh38
NC_000006.11:g.109268050C>T , CM000668.1:g.109268050C>T GRCh37
NC_000006.10:g.109374743C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392644.9:c.1597-6186C>T MANE Select ENSP00000376417.4:n.1597-6186C>T
ENST00000368972.7:c.1102-6186C>T ENSP00000357968.3:n.1102-6186C>T
ENST00000392644.8:c.1597-6186C>T ENSP00000376417.4:n.1597-6186C>T
NM_001286609.1:c.1102-6186C>T NP_001273538.1:n.1102-6186C>T
NM_032131.5:c.1597-6186C>T NP_115507.4:n.1597-6186C>T
XM_005267154.2:c.1597-6186C>T XP_005267211.1:n.1597-6186C>T
XM_005267155.2:c.1597-6186C>T XP_005267212.1:n.1597-6186C>T
XM_005267157.2:c.1102-6186C>T XP_005267214.1:n.1102-6186C>T
XM_006715573.2:c.1597-6186C>T XP_006715636.1:n.1597-6186C>T
XM_006715574.2:c.1102-6186C>T XP_006715637.1:n.1102-6186C>T
XM_011536166.1:c.1597-6186C>T XP_011534468.1:n.1597-6186C>T
XM_011536167.1:c.1597-6303C>T XP_011534469.1:n.1597-6303C>T
XM_011536168.1:c.1597-6186C>T XP_011534470.1:n.1597-6186C>T
XM_011536169.1:c.1597-6186C>T XP_011534471.1:n.1597-6186C>T
XM_011536170.1:c.1597-6186C>T XP_011534472.1:n.1597-6186C>T
XM_011536171.1:c.1270-6186C>T XP_011534473.1:n.1270-6186C>T
XM_011536172.1:c.1102-6186C>T XP_011534474.1:n.1102-6186C>T
XM_011536173.1:c.1597-6186C>T XP_011534475.1:n.1597-6186C>T
XM_011536174.1:c.856-6186C>T XP_011534476.1:n.856-6186C>T
XM_011536176.1:c.1497-6186C>T XP_011534478.1:n.1497-6186C>T
XM_005267154.4:c.1597-6186C>T XP_005267211.1:n.1597-6186C>T
XM_005267157.3:c.1102-6186C>T XP_005267214.1:n.1102-6186C>T
XM_011536168.3:c.1597-6186C>T XP_011534470.1:n.1597-6186C>T
XM_011536170.2:c.1597-6186C>T XP_011534472.1:n.1597-6186C>T
XM_011536172.2:c.1102-6186C>T XP_011534474.1:n.1102-6186C>T
XM_011536176.2:c.1497-6186C>T XP_011534478.1:n.1497-6186C>T
XM_017011350.1:c.856-6186C>T XP_016866839.1:n.856-6186C>T
XM_024446568.1:c.1102-6186C>T XP_024302336.1:n.1102-6186C>T
XR_001743676.1:n.2977C>T
NM_032131.6:c.1597-6186C>T MANE Select NP_115507.4:n.1597-6186C>T
NM_001286609.2:c.1102-6186C>T NP_001273538.1:n.1102-6186C>T