Canonical Allele Identifier: CA120661
Gene: SERPINA7 HGNC NCBI

Linked Data

ClinVar Variation Id: 9784
dbSNP Id: rs2234036

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106035377C>T , CM000685.2:g.106035377C>T GRCh38
NC_000023.10:g.105279368C>T , CM000685.1:g.105279368C>T GRCh37
NC_000023.9:g.105166024C>T NCBI36
NG_021252.1:g.8351G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372563.2:c.631G>A MANE Select ENSP00000361644.1:p.Ala211Thr
ENST00000327674.8:c.631G>A ENSP00000329374.4:p.Ala211Thr
ENST00000372563.1:c.631G>A ENSP00000361644.1:p.Ala211Thr
NM_000354.5:c.631G>A NP_000345.2:p.Ala211Thr
XM_005262180.3:c.631G>A XP_005262237.1:p.Ala211Thr
XM_006724683.1:c.631G>A XP_006724746.1:p.Ala211Thr
XM_005262180.4:c.631G>A XP_005262237.1:p.Ala211Thr
XM_006724683.2:c.631G>A XP_006724746.1:p.Ala211Thr
NM_000354.6:c.631G>A MANE Select NP_000345.2:p.Ala211Thr