Canonical Allele Identifier: CA327945235
Gene:

Linked Data

dbSNP Id: rs56156506
gnomAD v2: X-37999652-A-T
gnomAD v3: X-38140399-A-T
gnomAD v4: X-38140399-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38140399A>T , CM000685.2:g.38140399A>T GRCh38
NC_000023.10:g.37999652A>T , CM000685.1:g.37999652A>T GRCh37
NC_000023.9:g.37884596A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465127.1:c.172-525722A>T ENSP00000417050.1:n.172-525722A>T