Canonical Allele Identifier: CA869645372
Gene: SERPINA7 HGNC NCBI

Linked Data

dbSNP Id: rs1393541274
gnomAD v3: X-106033427-A-G
gnomAD v4: X-106033427-A-G
MyVariant Identifiers: chrX:g.105277418A>G (hg19) chrX:g.106033427A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106033427A>G , CM000685.2:g.106033427A>G GRCh38
NC_000023.10:g.105277418A>G , CM000685.1:g.105277418A>G GRCh37
NC_000023.9:g.105164074A>G NCBI36
NG_021252.1:g.10301T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372563.2:c.*73T>C MANE Select ENSP00000361644.1:n.*73T>C
ENST00000327674.8:c.*73T>C ENSP00000329374.4:n.*73T>C
ENST00000372563.1:c.*73T>C ENSP00000361644.1:n.*73T>C
NM_000354.5:c.*73T>C NP_000345.2:n.*73T>C
XM_006724683.1:c.*73T>C XP_006724746.1:n.*73T>C
XM_005262180.4:c.*266T>C XP_005262237.1:n.*266T>C
XM_006724683.2:c.*73T>C XP_006724746.1:n.*73T>C
NM_000354.6:c.*73T>C MANE Select NP_000345.2:n.*73T>C
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