Canonical Allele Identifier: CA2642120600
Gene: SERPINB7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63805262A>G , CM000680.2:g.63805262A>G GRCh38
NC_000018.9:g.61472496A>G , CM000680.1:g.61472496A>G GRCh37
NC_000018.8:g.59623476A>G NCBI36
NG_034150.1:g.57216A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398019.7:c.*627A>G MANE Select ENSP00000381101.2:n.*627A>G
ENST00000336429.6:c.*627A>G ENSP00000337212.2:n.*627A>G
ENST00000398019.6:c.*627A>G ENSP00000381101.2:n.*627A>G
ENST00000540675.5:c.*627A>G ENSP00000444572.1:n.*627A>G
ENST00000546027.5:c.*627A>G ENSP00000444861.1:n.*627A>G
NM_001040147.2:c.*627A>G NP_001035237.1:n.*627A>G
NM_001261830.1:c.*627A>G NP_001248759.1:n.*627A>G
NM_001261831.1:c.*627A>G NP_001248760.1:n.*627A>G
NM_003784.3:c.*627A>G NP_003775.1:n.*627A>G
XM_006722562.1:c.*627A>G XP_006722625.1:n.*627A>G
XM_011526236.1:c.*627A>G XP_011524538.1:n.*627A>G
XM_024451278.1:c.*627A>G XP_024307046.1:n.*627A>G
NM_003784.4:c.*627A>G MANE Select NP_003775.1:n.*627A>G
NM_001040147.3:c.*627A>G NP_001035237.1:n.*627A>G
NM_001261830.2:c.*627A>G NP_001248759.1:n.*627A>G
NM_001261831.2:c.*627A>G NP_001248760.1:n.*627A>G