Canonical Allele Identifier: CA2710665893
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs2113734520
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157515333T>G , CM000667.2:g.157515333T>G GRCh38
NC_000005.9:g.156942341T>G , CM000667.1:g.156942341T>G GRCh37
NC_000005.8:g.156874919T>G NCBI36
NG_046960.1:g.65491A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.667-1828A>C MANE Select ENSP00000257527.5:n.667-1828A>C
ENST00000257527.8:c.667-1828A>C ENSP00000257527.4:n.667-1828A>C
ENST00000517905.1:c.667-1828A>C ENSP00000428654.1:n.667-1828A>C
ENST00000517951.5:c.667-1828A>C ENSP00000428376.1:n.667-1828A>C
NM_033274.4:c.667-1828A>C NP_150377.1:n.667-1828A>C
XM_005266003.2:c.667-1828A>C XP_005266060.1:n.667-1828A>C
XM_011534680.1:c.-135-1828A>C XP_011532982.1:n.-135-1828A>C
XM_011534681.1:c.-145-1828A>C XP_011532983.1:n.-145-1828A>C
NM_033274.5:c.667-1828A>C MANE Select NP_150377.1:n.667-1828A>C
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