Canonical Allele Identifier: CA144309867
Gene:

Linked Data

dbSNP Id: rs138870726
gnomAD v2: 6-98462312-A-T
gnomAD v3: 6-98014436-A-T
gnomAD v4: 6-98014436-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014436A>T , CM000668.2:g.98014436A>T GRCh38
NC_000006.11:g.98462312A>T , CM000668.1:g.98462312A>T GRCh37
NC_000006.10:g.98569033A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+44970A>T
XR_942809.1:n.371+44970A>T