Canonical Allele Identifier: CA1083372808
Gene: ADAM19 HGNC NCBI

Linked Data

gnomAD v3: 5-157518127-A-G
gnomAD v4: 5-157518127-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157518127A>G , CM000667.2:g.157518127A>G GRCh38
NC_000005.9:g.156945135A>G , CM000667.1:g.156945135A>G GRCh37
NC_000005.8:g.156877713A>G NCBI36
NG_046960.1:g.62697T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.666+696T>C MANE Select ENSP00000257527.5:n.666+696T>C
ENST00000257527.8:c.666+696T>C ENSP00000257527.4:n.666+696T>C
ENST00000517905.1:c.666+696T>C ENSP00000428654.1:n.666+696T>C
ENST00000517951.5:c.666+696T>C ENSP00000428376.1:n.666+696T>C
NM_033274.4:c.666+696T>C NP_150377.1:n.666+696T>C
XM_005266003.2:c.666+696T>C XP_005266060.1:n.666+696T>C
XM_011534680.1:c.-135-4622T>C XP_011532982.1:n.-135-4622T>C
XM_011534681.1:c.-145-4622T>C XP_011532983.1:n.-145-4622T>C
NM_033274.5:c.666+696T>C MANE Select NP_150377.1:n.666+696T>C
Search 100 bp 5'
Search 100 bp 3'