Canonical Allele Identifier: CA174890876
Gene:

Linked Data

dbSNP Id: rs367804560
gnomAD v3: 8-31176543-T-C
gnomAD v4: 8-31176543-T-C
MyVariant Identifiers: chr8:g.31034059T>C (hg19) chr8:g.31176543T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176543T>C , CM000670.2:g.31176543T>C GRCh38
NC_000008.10:g.31034059T>C , CM000670.1:g.31034059T>C GRCh37
NC_000008.9:g.31153601T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949642.1:n.224T>C
XR_949643.1:n.87+149A>G
XR_949644.1:n.87+149A>G
XR_949645.1:n.87+149A>G
XR_949646.1:n.87+149A>G
XR_949647.1:n.700+149A>G
XR_949648.1:n.602+149A>G
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