Canonical Allele Identifier: CA88219491
Gene: SPATA16 HGNC NCBI

Linked Data

dbSNP Id: rs971376996
gnomAD v2: 3-172798812-C-G
gnomAD v3: 3-173081022-C-G
gnomAD v4: 3-173081022-C-G
MyVariant Identifiers: chr3:g.172798812C>G (hg19) chr3:g.173081022C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173081022C>G , CM000665.2:g.173081022C>G GRCh38
NC_000003.11:g.172798812C>G , CM000665.1:g.172798812C>G GRCh37
NC_000003.10:g.174281506C>G NCBI36
NG_021422.1:g.65247G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.613-31928G>C MANE Select ENSP00000341765.3:n.613-31928G>C
ENST00000351008.3:c.613-31928G>C ENSP00000341765.3:n.613-31928G>C
NM_031955.5:c.613-31928G>C NP_114161.3:n.613-31928G>C
XM_006713778.2:c.613-31928G>C XP_006713841.1:n.613-31928G>C
XM_011513222.1:c.613-31928G>C XP_011511524.1:n.613-31928G>C
XM_006713778.3:c.613-31928G>C XP_006713841.1:n.613-31928G>C
XM_017007308.2:c.613-31928G>C XP_016862797.1:n.613-31928G>C
NM_031955.6:c.613-31928G>C MANE Select NP_114161.3:n.613-31928G>C
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