Canonical Allele Identifier: CA648963368

Gene: ALB

Linked Data

• dbSNP Id: rs1718984115
• gnomAD v4: 4-73415202-G-T
• COSMIC: COSN1300854 ; COSN5063678

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415202G>T , CM000666.2:g.73415202G>T	GRCh38
NC_000004.11:g.74280919G>T , CM000666.1:g.74280919G>T	GRCh37
NC_000004.10:g.74499783G>T	NCBI36
NG_009291.1:g.15948G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1191+35G>T MANE Select	ENSP00000295897.4:n.1191+35G>T
ENST00000295897.8:c.1191+35G>T	ENSP00000295897.4:n.1191+35G>T
ENST00000401494.7:c.846+35G>T	ENSP00000384695.3:n.846+35G>T
ENST00000415165.6:c.615+35G>T	ENSP00000401820.2:n.615+35G>T
ENST00000476441.6:c.*470+35G>T	ENSP00000423727.1:n.*470+35G>T
ENST00000484992.1:n.511+35G>T
ENST00000503124.5:c.741+35G>T	ENSP00000421027.1:n.741+35G>T
ENST00000504043.1:n.229G>T
ENST00000505649.5:n.877+35G>T
ENST00000509063.5:c.1191+35G>T	ENSP00000422784.1:n.1191+35G>T
ENST00000511370.1:c.724+35G>T
ENST00000621085.4:c.552+35G>T	ENSP00000483421.1:n.552+35G>T
ENST00000621628.4:c.552+35G>T	ENSP00000480485.1:n.552+35G>T
NM_000477.5:c.1191+35G>T	NP_000468.1:n.1191+35G>T
NM_000477.6:c.1191+35G>T	NP_000468.1:n.1191+35G>T
NM_000477.7:c.1191+35G>T MANE Select	NP_000468.1:n.1191+35G>T